GONIOMETER AND BIOMEDICAL RECORDER SYSTEM
K-Number: K884003 · 1988-12-19
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Device Summary
Frequently Asked Questions
What is the GONIOMETER AND BIOMEDICAL RECORDER SYSTEM?
GONIOMETER AND BIOMEDICAL RECORDER SYSTEM is a medical device that received FDA 510(k) clearance on 1988-12-19. The listed applicant is Penny & Giles Blackwood , Ltd.. The 510(k) number is K884003.
When did GONIOMETER AND BIOMEDICAL RECORDER SYSTEM receive FDA 510(k) clearance?
GONIOMETER AND BIOMEDICAL RECORDER SYSTEM received FDA 510(k) clearance on 1988-12-19, under 510(k) number K884003.
Who is the listed applicant for GONIOMETER AND BIOMEDICAL RECORDER SYSTEM?
The FDA 510(k) record lists Penny & Giles Blackwood , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GONIOMETER AND BIOMEDICAL RECORDER SYSTEM?
The FDA product code for GONIOMETER AND BIOMEDICAL RECORDER SYSTEM is KQX.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: KQX)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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