FDA 510(k) clearance · back to tracker

TDX REA IRON DIAGNOSTIC KIT

Abbott Laboratories cleared K842505 on 1984-08-07, decision: substantially equivalent

K-number

K842505

Sponsor

Abbott Laboratories

Device

TDX REA IRON DIAGNOSTIC KIT

Class

Class I

Decision

Substantially Equivalent

Decision date

1984-08-07

Product code

CFM

Advisory committee

Clinical Chemistry

Medical specialty

Clinical Chemistry

Regulation number

862.1410

Official FDA record

Open K842505on 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 K842505 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.