FETAL BOVINE SERUM
K-Number: K800781 · 1980-04-21
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Device Summary
Frequently Asked Questions
What is the FETAL BOVINE SERUM?
FETAL BOVINE SERUM is a medical device that received FDA 510(k) clearance on 1980-04-21. The listed applicant is Biolabs, Inc.. The 510(k) number is K800781.
When did FETAL BOVINE SERUM receive FDA 510(k) clearance?
FETAL BOVINE SERUM received FDA 510(k) clearance on 1980-04-21, under 510(k) number K800781.
Who is the listed applicant for FETAL BOVINE SERUM?
The FDA 510(k) record lists Biolabs, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FETAL BOVINE SERUM?
The FDA product code for FETAL BOVINE SERUM is KIS.
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 Biolabs, 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: KIS)
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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