FDA 510(k) clearance · back to tracker

PROGESTERONE ASSAY FOR THE TECHNICON IMMUNO 1 SYSTEM IN-BITRO DIAGNOSTIC SYSTEM

Bayer Corp. cleared K952075 on 1995-06-13, decision: substantially equivalent

K-number

K952075

Sponsor

Bayer Corp.

Device

PROGESTERONE ASSAY FOR THE TECHNICON IMMUNO 1 SYSTEM IN-BITRO DIAGNOSTIC SYSTEM

Class

Class I

Decision

Substantially Equivalent

Decision date

1995-06-13

Product code

JLS

Advisory committee

Clinical Chemistry

Medical specialty

Clinical Chemistry

Regulation number

862.1620

Official FDA record

Open K952075on 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.

Use this as a predicate

Drop K952075 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.