MULTIHI-TEMP CAUTERY— 510(k) K810015

Name: FDA 510(k) clearance K810015
Creator: U.S. Food and Drug Administration
Published: 1981-02-12

Substantially Equivalent

Medical Products Development, Inc.

FDA 510(k) clearance K810015 for MULTIHI-TEMP CAUTERY, Substantially Equivalent on 1981-02-12. Applicant: Medical Products Development, Inc.. Device class: 2.

Clearance details

Applicant: Medical Products Development, Inc.
Product code: Code HAM
Device class: Class 2
Regulation: 21 CFR 878.4400
Advisory panel: General, Plastic Surgery
Date received: 1981-01-05
Decision date: 1981-02-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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More clearances from Medical Products Development, Inc.

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K810012 — MULTIMICRO SURGICAL CAUTERY1981-04-23
K810013 — MULTIPERFECTEMP CAUTERY1981-04-23
K810016 — REPLACABLE BATTERY PERFECTEMP CAUTERY1981-04-23
K803067 — SURG-FLEX 10 LIGHT1981-02-26
K810014 — REPLACABLE BATTERY HI-TEMP CAUTERY1981-02-12

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