SEPTI-CHEK BLOOD CULTURE BOTTLE ROCHE
K-Number: K812729 · 1981-10-19
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Device Summary
Frequently Asked Questions
What is the SEPTI-CHEK BLOOD CULTURE BOTTLE ROCHE?
SEPTI-CHEK BLOOD CULTURE BOTTLE ROCHE is a medical device that received FDA 510(k) clearance on 1981-10-19. The listed applicant is Hoffmann-La Roche, Inc.. The 510(k) number is K812729.
When did SEPTI-CHEK BLOOD CULTURE BOTTLE ROCHE receive FDA 510(k) clearance?
SEPTI-CHEK BLOOD CULTURE BOTTLE ROCHE received FDA 510(k) clearance on 1981-10-19, under 510(k) number K812729.
Who is the listed applicant for SEPTI-CHEK BLOOD CULTURE BOTTLE ROCHE?
The FDA 510(k) record lists Hoffmann-La Roche, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SEPTI-CHEK BLOOD CULTURE BOTTLE ROCHE?
The FDA product code for SEPTI-CHEK BLOOD CULTURE BOTTLE ROCHE is JSG.
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 Hoffmann-La Roche, 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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