RAPID DECARBOXYLASE/DIHYDROLASE MICROTUB
K-Number: K812469 · 1981-09-14
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Device Summary
Frequently Asked Questions
What is the RAPID DECARBOXYLASE/DIHYDROLASE MICROTUB?
RAPID DECARBOXYLASE/DIHYDROLASE MICROTUB is a medical device that received FDA 510(k) clearance on 1981-09-14. The listed applicant is Carr Microbiologicals. The 510(k) number is K812469.
When did RAPID DECARBOXYLASE/DIHYDROLASE MICROTUB receive FDA 510(k) clearance?
RAPID DECARBOXYLASE/DIHYDROLASE MICROTUB received FDA 510(k) clearance on 1981-09-14, under 510(k) number K812469.
Who is the listed applicant for RAPID DECARBOXYLASE/DIHYDROLASE MICROTUB?
The FDA 510(k) record lists Carr Microbiologicals as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RAPID DECARBOXYLASE/DIHYDROLASE MICROTUB?
The FDA product code for RAPID DECARBOXYLASE/DIHYDROLASE MICROTUB is JSF.
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 Carr Microbiologicals 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: JSF)
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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