FDA 510(k) clearance · back to tracker

ORION'S FOLEY CATHETERIZATION KIT WITH CATHETER AND BAG

Regulatory & Marketing Services, Inc. cleared K944379 on 1995-02-15, decision: substantially equivalent

K-number

K944379

Sponsor

Regulatory & Marketing Services, Inc.

Device

ORION'S FOLEY CATHETERIZATION KIT WITH CATHETER AND BAG

Class

Class I

Decision

Substantially Equivalent

Decision date

1995-02-15

Product code

FGM

Advisory committee

Gastroenterology, Urology

Medical specialty

Gastroenterology, Urology

Regulation number

876.4730

Official FDA record

Open K944379on accessdata.fda.gov →

FDA's authoritative 510(k) summary page. Includes the decision letter, predicate references, and downloadable substantial-equivalence determination.

openFDA JSON

Raw record →

Machine-readable JSON. Useful for cross-referencing classification, product code, and advisory committee fields.

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Drop K944379 into Compass and start a substantial-equivalence draft.

Compass pulls the predicate's intended use, technological characteristics, and performance data, maps them against your device, and produces a draft SE table aligned to FDA's 510(k) program guidance.

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Source

Public 510(k) database, U.S. Food and Drug Administration, accessed via openFDA. Page refreshed weekly.