VCA INHIBITOR— 510(k) K760589

Name: FDA 510(k) clearance K760589
Creator: U.S. Food and Drug Administration
Published: 1976-10-07

Substantially Equivalent

Bd Becton Dickinson Vacutainer Systems Preanalytic

FDA 510(k) clearance K760589 for VCA INHIBITOR, Substantially Equivalent on 1976-10-07. Applicant: Bd Becton Dickinson Vacutainer Systems Preanalytic. Device class: 1.

Clearance details

Applicant: Bd Becton Dickinson Vacutainer Systems Preanalytic
Product code: Code JSK
Device class: Class 1
Regulation: 21 CFR 866.2450
Advisory panel: Microbiology
Date received: 1976-09-03
Decision date: 1976-10-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code JSK

view all

K881949 — ATS NAC-PAC SET1988-05-25
K881879 — ATS M/15 PHOSPHATE BUFFER, PRODUCT #034-421988-05-13
K881566 — HEMOGLOBIN POWDER1988-04-18
K861997 — PENICILLIN-STREPTOMYCIN-FUNGIZONE MIXTURE1986-06-10
K861791 — PENICILLIN-STREPTOMYCIN-FUNGIZONE1986-05-20

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.