FDA 510(k) clearance · back to tracker

LEECO TESTOSTERONE DIAGNOSTIC KIT

Leeco Diagnostics, Inc. cleared K830512 on 1983-04-05, decision: substantially equivalent

K-number

K830512

Sponsor

Leeco Diagnostics, Inc.

Device

LEECO TESTOSTERONE DIAGNOSTIC KIT

Class

Class I

Decision

Substantially Equivalent

Decision date

1983-04-05

Product code

CDZ

Advisory committee

Clinical Chemistry

Medical specialty

Clinical Chemistry

Regulation number

862.1680

Official FDA record

Open K830512on 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 K830512 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.

Try the sandbox

Source

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