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FDA 510(k)

MRINNERVU DISPOSABLE ENDORECTAL COLON COIL,#PCC-15

K-Number: K930544 · 1993-09-29

ApplicantMedrad, Inc.
Decision Date1993-09-29
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MRINNERVU DISPOSABLE ENDORECTAL COLON COIL,#PCC-15 is the device name listed in this FDA 510(k) record. The listed applicant is Medrad, Inc.. It received FDA 510(k) clearance on 1993-09-29 under 510(k) number K930544. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MRINNERVU DISPOSABLE ENDORECTAL COLON COIL,#PCC-15?

MRINNERVU DISPOSABLE ENDORECTAL COLON COIL,#PCC-15 is a medical device that received FDA 510(k) clearance on 1993-09-29. The listed applicant is Medrad, Inc.. The 510(k) number is K930544.

When did MRINNERVU DISPOSABLE ENDORECTAL COLON COIL,#PCC-15 receive FDA 510(k) clearance?

MRINNERVU DISPOSABLE ENDORECTAL COLON COIL,#PCC-15 received FDA 510(k) clearance on 1993-09-29, under 510(k) number K930544.

Who is the listed applicant for MRINNERVU DISPOSABLE ENDORECTAL COLON COIL,#PCC-15?

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

What is the FDA product code for MRINNERVU DISPOSABLE ENDORECTAL COLON COIL,#PCC-15?

The FDA product code for MRINNERVU DISPOSABLE ENDORECTAL COLON COIL,#PCC-15 is LNH.

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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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