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FDA 510(k)

RAPID DECARBOXYLASE/DIHYDROLASE MICROTUB

K-Number: K812469 · 1981-09-14

Decision Date1981-09-14
Product CodeJSF
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

RAPID DECARBOXYLASE/DIHYDROLASE MICROTUB is the device name listed in this FDA 510(k) record. The listed applicant is Carr Microbiologicals. It received FDA 510(k) clearance on 1981-09-14 under 510(k) number K812469. The device is classified under product code JSF. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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