ANGIOMED SKIN FASCIA KNIFE— 510(k) K855104

Substantially Equivalent

Angiomed U.S., Inc.

FDA 510(k) clearance K855104 for ANGIOMED SKIN FASCIA KNIFE, Substantially Equivalent on 1986-01-24. Applicant: Angiomed U.S., Inc.. Device class: 1.

Clearance details

Applicant: Angiomed U.S., Inc.
Product code: Code GES
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1985-12-23
Decision date: 1986-01-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Anaheim, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code GES

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K932998 — EASY-ON1993-08-18
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K915119 — SCALPEL BLADE REMOVER (BLADEGARD)1992-05-05
K911913 — PRECISION GLIDE - ENHANCED SURGICAL BLADE1991-05-13

More clearances from Angiomed U.S., Inc.

K874771 — ANGIOMED INTRODUCING SETS1988-01-12
K874585 — ANGIOMED OSTY-CUT BONE BIOPSY NEEDLE1987-12-02
K864225 — ANGIOMED URETERAL D&M SETS/URETEROSCOPY GUID STENT1987-01-30
K863386 — VESICO SUPRAPUBIC BLADDER DRAINAGE & EXCHANGE SETS1986-10-24
K862805 — ANGIOMED VAC-U-CUT BIOPSY NEEDLE1986-09-29

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