IDENTI-CLAMPS
K-Number: K780721 · 1978-10-17
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Device Summary
Frequently Asked Questions
What is the IDENTI-CLAMPS?
IDENTI-CLAMPS is a medical device that received FDA 510(k) clearance on 1978-10-17. The listed applicant is Berkeley Bio-Medical, Inc.. The 510(k) number is K780721.
When did IDENTI-CLAMPS receive FDA 510(k) clearance?
IDENTI-CLAMPS received FDA 510(k) clearance on 1978-10-17, under 510(k) number K780721.
Who is the listed applicant for IDENTI-CLAMPS?
The FDA 510(k) record lists Berkeley Bio-Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for IDENTI-CLAMPS?
The FDA product code for IDENTI-CLAMPS is GDJ.
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 Berkeley Bio-Medical, 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: GDJ)
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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