KEISEI SCALPEL (STERILE AND NON-STERILE)— 510(k) K863213

Name: FDA 510(k) clearance K863213
Creator: U.S. Food and Drug Administration
Published: 1986-09-02

Substantially Equivalent

Keisei Medical Industrial Co., Ltd.

FDA 510(k) clearance K863213 for KEISEI SCALPEL (STERILE AND NON-STERILE), Substantially Equivalent on 1986-09-02. Applicant: Keisei Medical Industrial Co., Ltd.. Device class: 1.

Clearance details

Applicant: Keisei Medical Industrial Co., Ltd.
Product code: Code GDX
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1986-08-20
Decision date: 1986-09-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bethel, CT, US

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More clearances from Keisei Medical Industrial Co., Ltd.

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K863211 — KEISEI SURGICAL BLADES (STERILE & NON-STERILE)1986-09-02
K863212 — KEISEI HANDLES FOR SURGICAL BLADES1986-09-02
K863214 — KEISEI MICRO-BLADES (STERILE AND NON-STERILE)1986-09-02

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