FDA 510(k) clearance · back to tracker

NAVARRE UNIVERSAL DRAINAGE CATHETER

Navarre Biomedical , Ltd. cleared K951475 on 1995-04-24, decision: substantially equivalent

K-number

K951475

Sponsor

Navarre Biomedical , Ltd.

Device

NAVARRE UNIVERSAL DRAINAGE CATHETER

Class

Class I

Decision

Substantially Equivalent

Decision date

1995-04-24

Product code

GBX

Advisory committee

General, Plastic Surgery

Medical specialty

General, Plastic Surgery

Regulation number

878.4200

Official FDA record

Open K951475on accessdata.fda.gov →

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

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

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Source

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