VERSA-VIAL— 510(k) K920177

Substantially Equivalent

Bioteque America, Inc.

FDA 510(k) clearance K920177 for VERSA-VIAL, Substantially Equivalent on 1992-07-13. Applicant: Bioteque America, Inc.. Device class: 2.

Clearance details

Applicant: Bioteque America, Inc.
Product code: Code DQF
Device class: Class 2
Regulation: 21 CFR 870.1670
Advisory panel: Cardiovascular
Date received: 1992-01-14
Decision date: 1992-07-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Levittown, PA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code DQF

K882723 — ALCON FLUID INJECTOR1988-11-08
K880740 — MODEL TA-CS10 SPECTRAJECT CONTROL SYRINGE1988-03-22

More clearances from Bioteque America, Inc.

K041094 — HSG CATHETER SET2004-06-17
K020628 — CURELLE, PREFERRED CURELLE, CUTEQ 2.52002-05-24
K013289 — BIOTEQUE VAGINAL PESSARIES2001-12-27
K003380 — BIOTEQUE VAGINAL DILATOR2001-01-29
K920633 — PESSARY FLEXIBLE SILICONE NICHOLS1995-11-08

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