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FDA 510(k)

AGGLUTINOTEST-PERTUSSIS

K-Number: K791454 · 1979-09-24

ApplicantVolu Sol Medical Industries
Decision Date1979-09-24
Product CodeGOX
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

AGGLUTINOTEST-PERTUSSIS is the device name listed in this FDA 510(k) record. The listed applicant is Volu Sol Medical Industries. It received FDA 510(k) clearance on 1979-09-24 under 510(k) number K791454. The device is classified under product code GOX. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AGGLUTINOTEST-PERTUSSIS?

AGGLUTINOTEST-PERTUSSIS is a medical device that received FDA 510(k) clearance on 1979-09-24. The listed applicant is Volu Sol Medical Industries. The 510(k) number is K791454.

When did AGGLUTINOTEST-PERTUSSIS receive FDA 510(k) clearance?

AGGLUTINOTEST-PERTUSSIS received FDA 510(k) clearance on 1979-09-24, under 510(k) number K791454.

Who is the listed applicant for AGGLUTINOTEST-PERTUSSIS?

The FDA 510(k) record lists Volu Sol Medical Industries as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AGGLUTINOTEST-PERTUSSIS?

The FDA product code for AGGLUTINOTEST-PERTUSSIS is GOX.

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Other records listing Volu Sol Medical Industries 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.

K822128VOLU-SOL SINGLE DIFFERENTIAL STAINK822127VOLU-SOL ZENKERS FIXATIVEK822126VOLU-SOL CARNOY FLUIDK822129VOLU-SOL BOVINS FIXATIVEK822036VOLU-SOL DECALCIFERK822035VOLU-SOL GILLS EA

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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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