GONIOMETER AND BIOMEDICAL RECORDER SYSTEM— 510(k) K884003

Name: FDA 510(k) clearance K884003
Creator: U.S. Food and Drug Administration
Published: 1988-12-19

Substantially Equivalent

Penny & Giles Blackwood , Ltd.

FDA 510(k) clearance K884003 for GONIOMETER AND BIOMEDICAL RECORDER SYSTEM, Substantially Equivalent on 1988-12-19. Applicant: Penny & Giles Blackwood , Ltd.. Device class: 1.

Clearance details

Applicant: Penny & Giles Blackwood , Ltd.
Product code: Code KQX
Device class: Class 1
Regulation: 21 CFR 888.1500
Advisory panel: Orthopedic
Date received: 1988-09-21
Decision date: 1988-12-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: England, GB

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