FDA 510(k) clearance · back to tracker

TBG DIAGNOSTIC KIT

Immuno Assay Corp. cleared K811725 on 1981-07-10, decision: substantially equivalent

K-number

K811725

Sponsor

Immuno Assay Corp.

Device

TBG DIAGNOSTIC KIT

Class

Class I

Decision

Substantially Equivalent

Decision date

1981-07-10

Product code

CEF

Advisory committee

Clinical Chemistry

Medical specialty

Clinical Chemistry

Regulation number

862.1630

Official FDA record

Open K811725on 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 K811725 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.