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FDA 510(k)

FILTRESSE, SMOKE FILTRATION SYSTEM, 115 VAC & 230 VAC

K-Number: K952981 · 1995-08-28

ApplicantUtah Medical Products, Inc.
Decision Date1995-08-28
Product CodeFYD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

FILTRESSE, SMOKE FILTRATION SYSTEM, 115 VAC & 230 VAC is the device name listed in this FDA 510(k) record. The listed applicant is Utah Medical Products, Inc.. It received FDA 510(k) clearance on 1995-08-28 under 510(k) number K952981. The device is classified under product code FYD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FILTRESSE, SMOKE FILTRATION SYSTEM, 115 VAC & 230 VAC?

FILTRESSE, SMOKE FILTRATION SYSTEM, 115 VAC & 230 VAC is a medical device that received FDA 510(k) clearance on 1995-08-28. The listed applicant is Utah Medical Products, Inc.. The 510(k) number is K952981.

When did FILTRESSE, SMOKE FILTRATION SYSTEM, 115 VAC & 230 VAC receive FDA 510(k) clearance?

FILTRESSE, SMOKE FILTRATION SYSTEM, 115 VAC & 230 VAC received FDA 510(k) clearance on 1995-08-28, under 510(k) number K952981.

Who is the listed applicant for FILTRESSE, SMOKE FILTRATION SYSTEM, 115 VAC & 230 VAC?

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

What is the FDA product code for FILTRESSE, SMOKE FILTRATION SYSTEM, 115 VAC & 230 VAC?

The FDA product code for FILTRESSE, SMOKE FILTRATION SYSTEM, 115 VAC & 230 VAC is FYD.

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Other records listing Utah Medical Products, Inc. as applicant

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Related Devices (Code: FYD)

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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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