MICROSURG CAUTERY— 510(k) K810017

Unknown

Medical Products Development, Inc.

FDA 510(k) clearance K810017 for MICROSURG CAUTERY, Unknown on 1981-01-05. Applicant: Medical Products Development, Inc.. Device class: 2.

Clearance details

Applicant: Medical Products Development, Inc.
Product code: Code HQO
Device class: Class 2
Regulation: 21 CFR 886.4115
Advisory panel: Ophthalmic
Date received: 1981-01-05
Decision date: 1981-01-05
Decision: Unknown
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.

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

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