BETA-CELL
K-Number: K791607 · 1979-09-24
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Device Summary
Frequently Asked Questions
What is the BETA-CELL?
BETA-CELL is a medical device that received FDA 510(k) clearance on 1979-09-24. The listed applicant is Biologics Intl., Inc.. The 510(k) number is K791607.
When did BETA-CELL receive FDA 510(k) clearance?
BETA-CELL received FDA 510(k) clearance on 1979-09-24, under 510(k) number K791607.
Who is the listed applicant for BETA-CELL?
The FDA 510(k) record lists Biologics Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BETA-CELL?
The FDA product code for BETA-CELL is JSG.
Other records listing Biologics Intl., 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: JSG)
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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