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FDA 510(k)

STERIVENT AND STERIVENT S

K-Number: K941676 · 1994-05-20

ApplicantMallinckrodt Medical
Decision Date1994-05-20
Product CodeCAH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

STERIVENT AND STERIVENT S is the device name listed in this FDA 510(k) record. The listed applicant is Mallinckrodt Medical. It received FDA 510(k) clearance on 1994-05-20 under 510(k) number K941676. The device is classified under product code CAH. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STERIVENT AND STERIVENT S?

STERIVENT AND STERIVENT S is a medical device that received FDA 510(k) clearance on 1994-05-20. The listed applicant is Mallinckrodt Medical. The 510(k) number is K941676.

When did STERIVENT AND STERIVENT S receive FDA 510(k) clearance?

STERIVENT AND STERIVENT S received FDA 510(k) clearance on 1994-05-20, under 510(k) number K941676.

Who is the listed applicant for STERIVENT AND STERIVENT S?

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

What is the FDA product code for STERIVENT AND STERIVENT S?

The FDA product code for STERIVENT AND STERIVENT S is CAH.

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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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