VAN-TEC BLADDER EVACUATOR— 510(k) K880099

Substantially Equivalent

Van-Tec, Inc.

FDA 510(k) clearance K880099 for VAN-TEC BLADDER EVACUATOR, Substantially Equivalent on 1988-03-02. Applicant: Van-Tec, Inc.. Device class: 2.

Clearance details

Applicant: Van-Tec, Inc.
Product code: Code KQT
Device class: Class 2
Regulation: 21 CFR 876.4370
Advisory panel: Gastroenterology, Urology
Date received: 1988-01-12
Decision date: 1988-03-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Spencer, IN, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KQT

K964111 — LITHOVAC SUCTION/ASPIRATION PROBE1996-12-16
K921088 — EVACUATOR, GASTRO-UROLOGY1992-10-28
K921451 — EVACUATOR, GASTRO-UROLOGY1992-10-28
K910728 — CLEANFLOW SYSTEM1991-04-01
K874493 — BELLA - VAC IRRIGATOR1988-02-05

More clearances from Van-Tec, Inc.

K880095 — BERGER PROSTATE CULTURE CYTOLOGY BRUSH1988-03-02
K880096 — VAN-TEC ASPIRATION BIOPSY SYSTEM W/COLLECTION CUP1988-03-02
K880098 — VAN-TEC AUTO BIOPSY NEEDLE1988-03-02
K880094 — VAN-TEC ENDOPYELOTOMY KNIFE1988-02-29
K874112 — VAN-TEC DOUBLE OCCLUSION BALLOON CATHETER1988-02-11

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