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FDA 510(k)

AUDIOPRAT ENDOSCOPE

K-Number: K903012 · 1990-10-09

ApplicantS.C.D.P.I. of Florida, Inc.
Decision Date1990-10-09
Product CodeEHB
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

AUDIOPRAT ENDOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is S.C.D.P.I. of Florida, Inc.. It received FDA 510(k) clearance on 1990-10-09 under 510(k) number K903012. The device is classified under product code EHB. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUDIOPRAT ENDOSCOPE?

AUDIOPRAT ENDOSCOPE is a medical device that received FDA 510(k) clearance on 1990-10-09. The listed applicant is S.C.D.P.I. of Florida, Inc.. The 510(k) number is K903012.

When did AUDIOPRAT ENDOSCOPE receive FDA 510(k) clearance?

AUDIOPRAT ENDOSCOPE received FDA 510(k) clearance on 1990-10-09, under 510(k) number K903012.

Who is the listed applicant for AUDIOPRAT ENDOSCOPE?

The FDA 510(k) record lists S.C.D.P.I. of Florida, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AUDIOPRAT ENDOSCOPE?

The FDA product code for AUDIOPRAT ENDOSCOPE is EHB.

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Related Devices (Code: EHB)

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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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