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FDA 510(k)

IMMUNOFLUORESCENCE TEST KIT

K-Number: K781143 · 1978-08-14

ApplicantMicrobiological Assoc.
Decision Date1978-08-14
Product Code
DecisionSubstantially Equivalent

Device Summary

IMMUNOFLUORESCENCE TEST KIT is the device name listed in this FDA 510(k) record. The listed applicant is Microbiological Assoc.. It received FDA 510(k) clearance on 1978-08-14 under 510(k) number K781143. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IMMUNOFLUORESCENCE TEST KIT?

IMMUNOFLUORESCENCE TEST KIT is a medical device that received FDA 510(k) clearance on 1978-08-14. The listed applicant is Microbiological Assoc.. The 510(k) number is K781143.

When did IMMUNOFLUORESCENCE TEST KIT receive FDA 510(k) clearance?

IMMUNOFLUORESCENCE TEST KIT received FDA 510(k) clearance on 1978-08-14, under 510(k) number K781143.

Who is the listed applicant for IMMUNOFLUORESCENCE TEST KIT?

The FDA 510(k) record lists Microbiological Assoc. as the applicant. This does not by itself establish the device manufacturer.

Related Clinical Trials

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Other records listing Microbiological Assoc. 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.

K792133RUBELISA TEST KITK791397HERPES EIA TEST KITK781549TOXELISA TEST KITK780996RUBELISA TEST KITK781392CYTOMEGILISH TEST KITK770764TISSUE CULTURE MEDIA W/HEPES BUFFER

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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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