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FDA 510(k)

MEASLES-COMPLEMENT FIX ANTIGEN & NEGATIVE CLT

K-Number: K852932 · 1985-11-12

ApplicantMicrobix Biosystems, Inc.
Decision Date1985-11-12
Product CodeGRF
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

MEASLES-COMPLEMENT FIX ANTIGEN & NEGATIVE CLT is the device name listed in this FDA 510(k) record. The listed applicant is Microbix Biosystems, Inc.. It received FDA 510(k) clearance on 1985-11-12 under 510(k) number K852932. The device is classified under product code GRF. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEASLES-COMPLEMENT FIX ANTIGEN & NEGATIVE CLT?

MEASLES-COMPLEMENT FIX ANTIGEN & NEGATIVE CLT is a medical device that received FDA 510(k) clearance on 1985-11-12. The listed applicant is Microbix Biosystems, Inc.. The 510(k) number is K852932.

When did MEASLES-COMPLEMENT FIX ANTIGEN & NEGATIVE CLT receive FDA 510(k) clearance?

MEASLES-COMPLEMENT FIX ANTIGEN & NEGATIVE CLT received FDA 510(k) clearance on 1985-11-12, under 510(k) number K852932.

Who is the listed applicant for MEASLES-COMPLEMENT FIX ANTIGEN & NEGATIVE CLT?

The FDA 510(k) record lists Microbix Biosystems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEASLES-COMPLEMENT FIX ANTIGEN & NEGATIVE CLT?

The FDA product code for MEASLES-COMPLEMENT FIX ANTIGEN & NEGATIVE CLT is GRF.

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Other records listing Microbix Biosystems, 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.

K894262RUBELLA ANTIGEN AND CONTROL ANTIGENK894261TOXOPLASMA GONDII-CF ANTIGEN AND CONTROL ANTIGENK852930VARICELLA-ZOSTER-COMPLE FIX ANTIGEN AND NEG CONTROK852929CMV-COMPLEMENT FIXATION ANTIGEN AND NEGATIVE CONTRK852931HERPES HOMINUS I-COMPLE FIX ANTIGEN & NEGATIVE CLTK852933MYCOPLASMA SPP SEROLOGICAL REAGENTS

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Related Devices (Code: GRF)

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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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