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FDA 510(k)

STERI-TAMP

K-Number: K974180 · 1998-02-24

ApplicantPharmacy, Inc.
Decision Date1998-02-24
Product CodeKPE
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

STERI-TAMP is the device name listed in this FDA 510(k) record. The listed applicant is Pharmacy, Inc.. It received FDA 510(k) clearance on 1998-02-24 under 510(k) number K974180. The device is classified under product code KPE. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STERI-TAMP?

STERI-TAMP is a medical device that received FDA 510(k) clearance on 1998-02-24. The listed applicant is Pharmacy, Inc.. The 510(k) number is K974180.

When did STERI-TAMP receive FDA 510(k) clearance?

STERI-TAMP received FDA 510(k) clearance on 1998-02-24, under 510(k) number K974180.

Who is the listed applicant for STERI-TAMP?

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

What is the FDA product code for STERI-TAMP?

The FDA product code for STERI-TAMP is KPE.

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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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