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FDA 510(k)

MUCUS ASPIRATOR

K-Number: K781917 · 1978-12-04

ApplicantOvutime, Inc.
Decision Date1978-12-04
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MUCUS ASPIRATOR is the device name listed in this FDA 510(k) record. The listed applicant is Ovutime, Inc.. It received FDA 510(k) clearance on 1978-12-04 under 510(k) number K781917. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MUCUS ASPIRATOR?

MUCUS ASPIRATOR is a medical device that received FDA 510(k) clearance on 1978-12-04. The listed applicant is Ovutime, Inc.. The 510(k) number is K781917.

When did MUCUS ASPIRATOR receive FDA 510(k) clearance?

MUCUS ASPIRATOR received FDA 510(k) clearance on 1978-12-04, under 510(k) number K781917.

Who is the listed applicant for MUCUS ASPIRATOR?

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

What is the FDA product code for MUCUS ASPIRATOR?

The FDA product code for MUCUS ASPIRATOR is FMF.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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