VAN-TEC ENDOPYELOTOMY KNIFE— 510(k) K880094

Substantially Equivalent

Van-Tec, Inc.

FDA 510(k) clearance K880094 for VAN-TEC ENDOPYELOTOMY KNIFE, Substantially Equivalent on 1988-02-29. Applicant: Van-Tec, Inc.. Device class: 1.

Clearance details

Applicant: Van-Tec, Inc.
Product code: Code EMF
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1988-01-12
Decision date: 1988-02-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Spencer, IN, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code EMF

K080133 — MOUNTABLE ENDOSCOPIC BLADE2008-03-13
K982142 — MOUNTABLE ENDOSCOPIC KNIFE1998-12-30
K890214 — MICROSURGERY RAZOR BLADE HOLDER1989-01-27
K890215 — MICROSURGICAL SCARIFIER1989-01-27
K890217 — MICROSURGICAL KNIVES1989-01-27

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
K880099 — VAN-TEC BLADDER EVACUATOR1988-03-02
K874112 — VAN-TEC DOUBLE OCCLUSION BALLOON CATHETER1988-02-11

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