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FDA 510(k)

NORSEN DEBRIDER

K-Number: K821801 · 1982-07-28

ApplicantBel-Med, Inc.
Decision Date1982-07-28
Product CodeGED
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

NORSEN DEBRIDER is the device name listed in this FDA 510(k) record. The listed applicant is Bel-Med, Inc.. It received FDA 510(k) clearance on 1982-07-28 under 510(k) number K821801. The device is classified under product code GED. 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 1982-07-28. The listed applicant is Bel-Med, Inc.. The 510(k) number is K821801.

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

NORSEN DEBRIDER received FDA 510(k) clearance on 1982-07-28, under 510(k) number K821801.

Who is the listed applicant for NORSEN DEBRIDER?

The FDA 510(k) record lists Bel-Med, 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 GED.

Related Clinical Trials

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Other records listing Bel-Med, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K770426OXYGEN MANIFOLD SYSTEMS, NITROUS OXIDE

Related Devices (Code: GED)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K830259PROTET SOAP & WASH MITTRitmed, Inc.

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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