CAMPYPAK PLUS W/PALLADIUM CATALYST DISPOS. HYDROGE— 510(k) K844571

Name: FDA 510(k) clearance K844571
Creator: U.S. Food and Drug Administration
Published: 1985-01-30

Substantially Equivalent

Bd Becton Dickinson Vacutainer Systems Preanalytic

FDA 510(k) clearance K844571 for CAMPYPAK PLUS W/PALLADIUM CATALYST DISPOS. HYDROGE, Substantially Equivalent on 1985-01-30. Applicant: Bd Becton Dickinson Vacutainer Systems Preanalytic. Device class: 1.

Clearance details

Applicant: Bd Becton Dickinson Vacutainer Systems Preanalytic
Product code: Code KZJ
Device class: Class 1
Regulation: 21 CFR 866.2580
Advisory panel: Microbiology
Date received: 1984-11-23
Decision date: 1985-01-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KZJ

view all

K881502 — BREWER GEL FOR CAMPYLOBACTER1988-04-27
K875362 — BREWER GEL FOR ANAEROBES1988-01-27
K872782 — BBL(R) GASPAK CO2 POUCH(TM)1987-08-06
K871709 — ANAEROBIC TRANSPORT POUCH (CATALYST-FREE)1987-05-15
K871238 — ANABAG1987-04-03

More clearances from Bd Becton Dickinson Vacutainer Systems Preanalytic

view all

K003062 — BACTEC MGIT 960 SIR KITS2001-06-06
K003553 — 0.9% SODIUM CHLORIDE INJECTION, USP BD PRE-FILLED FLUSH SYRINGE2001-03-21
K003461 — BD VACUTAINER PASSIVE SHIELDING BLOOD COLLECTION NEEDLE2001-02-01
K002938 — B-D ULTRA-FINE III PEN NEEDLE; MODEL 31G X 3/162000-11-29
K001364 — BD DIRECTIGEN FLU A+B2000-06-28

Data sourced from openFDA. This site is unofficial and independent of the FDA.