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FDA 510(k)

CULTURETTE BRAND PVA

K-Number: K790815 · 1979-05-15

ApplicantMarion Laboratories, Inc.
Decision Date1979-05-15
Product CodeIGM
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

CULTURETTE BRAND PVA is the device name listed in this FDA 510(k) record. The listed applicant is Marion Laboratories, Inc.. It received FDA 510(k) clearance on 1979-05-15 under 510(k) number K790815. The device is classified under product code IGM. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CULTURETTE BRAND PVA?

CULTURETTE BRAND PVA is a medical device that received FDA 510(k) clearance on 1979-05-15. The listed applicant is Marion Laboratories, Inc.. The 510(k) number is K790815.

When did CULTURETTE BRAND PVA receive FDA 510(k) clearance?

CULTURETTE BRAND PVA received FDA 510(k) clearance on 1979-05-15, under 510(k) number K790815.

Who is the listed applicant for CULTURETTE BRAND PVA?

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

What is the FDA product code for CULTURETTE BRAND PVA?

The FDA product code for CULTURETTE BRAND PVA is IGM.

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Other records listing Marion Laboratories, Inc. as applicant

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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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