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FDA 510(k)

NORSEN DEBRIDER

K-Number: K800647 · 1980-04-16

ApplicantMedline Industries, Inc.
Decision Date1980-04-16
Product CodeGEN
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

NORSEN DEBRIDER is the device name listed in this FDA 510(k) record. The listed applicant is Medline Industries, Inc.. It received FDA 510(k) clearance on 1980-04-16 under 510(k) number K800647. The device is classified under product code GEN. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NORSEN DEBRIDER?

NORSEN DEBRIDER is a medical device that received FDA 510(k) clearance on 1980-04-16. The listed applicant is Medline Industries, Inc.. The 510(k) number is K800647.

When did NORSEN DEBRIDER receive FDA 510(k) clearance?

NORSEN DEBRIDER received FDA 510(k) clearance on 1980-04-16, under 510(k) number K800647.

Who is the listed applicant for NORSEN DEBRIDER?

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

What is the FDA product code for NORSEN DEBRIDER?

The FDA product code for NORSEN DEBRIDER is GEN.

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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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