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FDA 510(k)

HPM REPLACEMENT ULPA FILTER MODEL UF001

K-Number: K920371 · 1992-08-12

ApplicantHpm Ent.
Decision Date1992-08-12
Product CodeFYD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

HPM REPLACEMENT ULPA FILTER MODEL UF001 is the device name listed in this FDA 510(k) record. The listed applicant is Hpm Ent.. It received FDA 510(k) clearance on 1992-08-12 under 510(k) number K920371. 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 HPM REPLACEMENT ULPA FILTER MODEL UF001?

HPM REPLACEMENT ULPA FILTER MODEL UF001 is a medical device that received FDA 510(k) clearance on 1992-08-12. The listed applicant is Hpm Ent.. The 510(k) number is K920371.

When did HPM REPLACEMENT ULPA FILTER MODEL UF001 receive FDA 510(k) clearance?

HPM REPLACEMENT ULPA FILTER MODEL UF001 received FDA 510(k) clearance on 1992-08-12, under 510(k) number K920371.

Who is the listed applicant for HPM REPLACEMENT ULPA FILTER MODEL UF001?

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

What is the FDA product code for HPM REPLACEMENT ULPA FILTER MODEL UF001?

The FDA product code for HPM REPLACEMENT ULPA FILTER MODEL UF001 is 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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