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FDA 510(k)

VAGINALIS, HAEMOPHILUS

K-Number: K790229 · 1979-02-26

ApplicantLos Angeles Biological Products
Decision Date1979-02-26
Product CodeJSH
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

VAGINALIS, HAEMOPHILUS is the device name listed in this FDA 510(k) record. The listed applicant is Los Angeles Biological Products. It received FDA 510(k) clearance on 1979-02-26 under 510(k) number K790229. The device is classified under product code JSH. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VAGINALIS, HAEMOPHILUS?

VAGINALIS, HAEMOPHILUS is a medical device that received FDA 510(k) clearance on 1979-02-26. The listed applicant is Los Angeles Biological Products. The 510(k) number is K790229.

When did VAGINALIS, HAEMOPHILUS receive FDA 510(k) clearance?

VAGINALIS, HAEMOPHILUS received FDA 510(k) clearance on 1979-02-26, under 510(k) number K790229.

Who is the listed applicant for VAGINALIS, HAEMOPHILUS?

The FDA 510(k) record lists Los Angeles Biological Products as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VAGINALIS, HAEMOPHILUS?

The FDA product code for VAGINALIS, HAEMOPHILUS is JSH.

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Other records listing Los Angeles Biological Products 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.

K790230DENTRIFICATION LACTOSE AGARK790231DECARBOXYLASE, BUFFERED LYSINEK790232AGAR, MOTILITY-NITRATE

Related Devices (Code: JSH)

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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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