FDA 510(k) clearance · back to tracker

XENOSTRIP-TV TRICHOMONAS DIAGNOSTIC TEST KIT; CATALOG NUMBERS S1383.01, S1383.02 & S1383.03

Hellen Professional Services cleared K020226 on 2002-08-22, decision: substantially equivalent

K-number

K020226

Sponsor

Hellen Professional Services

Device

XENOSTRIP-TV TRICHOMONAS DIAGNOSTIC TEST KIT; CATALOG NUMBERS S1383.01, S1383.02 & S1383.03

Class

Class I

Decision

Substantially Equivalent

Decision date

2002-08-22

Product code

JWZ

Advisory committee

Microbiology

Medical specialty

Microbiology

Regulation number

866.2660

Official FDA record

Open K020226on 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 K020226 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.