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FDA 510(k)

PHOENIX STERI-TECH STERILE DENTAL PACK GEN-10001

K-Number: K920682 · 1992-04-28

ApplicantPhoenix Steri-Tech, Inc.
Decision Date1992-04-28
Product CodeFXX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PHOENIX STERI-TECH STERILE DENTAL PACK GEN-10001 is the device name listed in this FDA 510(k) record. The listed applicant is Phoenix Steri-Tech, Inc.. It received FDA 510(k) clearance on 1992-04-28 under 510(k) number K920682. The device is classified under product code FXX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PHOENIX STERI-TECH STERILE DENTAL PACK GEN-10001?

PHOENIX STERI-TECH STERILE DENTAL PACK GEN-10001 is a medical device that received FDA 510(k) clearance on 1992-04-28. The listed applicant is Phoenix Steri-Tech, Inc.. The 510(k) number is K920682.

When did PHOENIX STERI-TECH STERILE DENTAL PACK GEN-10001 receive FDA 510(k) clearance?

PHOENIX STERI-TECH STERILE DENTAL PACK GEN-10001 received FDA 510(k) clearance on 1992-04-28, under 510(k) number K920682.

Who is the listed applicant for PHOENIX STERI-TECH STERILE DENTAL PACK GEN-10001?

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

What is the FDA product code for PHOENIX STERI-TECH STERILE DENTAL PACK GEN-10001?

The FDA product code for PHOENIX STERI-TECH STERILE DENTAL PACK GEN-10001 is FXX.

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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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