GONIOMETER, MED. INTER. STAND. BK-7512
K-Number: K760301 · 1976-09-08
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Device Summary
Frequently Asked Questions
What is the GONIOMETER, MED. INTER. STAND. BK-7512?
GONIOMETER, MED. INTER. STAND. BK-7512 is a medical device that received FDA 510(k) clearance on 1976-09-08. The listed applicant is Fred Sammons, Inc.. The 510(k) number is K760301.
When did GONIOMETER, MED. INTER. STAND. BK-7512 receive FDA 510(k) clearance?
GONIOMETER, MED. INTER. STAND. BK-7512 received FDA 510(k) clearance on 1976-09-08, under 510(k) number K760301.
Who is the listed applicant for GONIOMETER, MED. INTER. STAND. BK-7512?
The FDA 510(k) record lists Fred Sammons, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GONIOMETER, MED. INTER. STAND. BK-7512?
The FDA product code for GONIOMETER, MED. INTER. STAND. BK-7512 is KQW.
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.
Other records listing Fred Sammons, Inc. as applicant
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: KQW)
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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