GONIOMETER, MED. INTER. STAND. BK-7512— 510(k) K760301

Name: FDA 510(k) clearance K760301
Creator: U.S. Food and Drug Administration
Published: 1976-09-08

Substantially Equivalent

Fred Sammons, Inc.

FDA 510(k) clearance K760301 for GONIOMETER, MED. INTER. STAND. BK-7512, Substantially Equivalent on 1976-09-08. Applicant: Fred Sammons, Inc.. Device class: 1.

Clearance details

Applicant: Fred Sammons, Inc.
Product code: Code KQW
Device class: Class 1
Regulation: 21 CFR 888.1520
Advisory panel: Orthopedic
Date received: 1976-07-23
Decision date: 1976-09-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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K831550 — FINGER BONIOMETER BK75061983-06-24

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K831548 — SPLINTS1983-06-27
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