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FDA 510(k)

NU-GEL * WOUND DRESSING

K-Number: K983362 · 1998-12-16

ApplicantJohnson & Johnson Medical, Inc.
Decision Date1998-12-16
Product CodeMGQ
DecisionSubstantially Equivalent

Device Summary

NU-GEL * WOUND DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Johnson & Johnson Medical, Inc.. It received FDA 510(k) clearance on 1998-12-16 under 510(k) number K983362. The device is classified under product code MGQ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NU-GEL * WOUND DRESSING?

NU-GEL * WOUND DRESSING is a medical device that received FDA 510(k) clearance on 1998-12-16. The listed applicant is Johnson & Johnson Medical, Inc.. The 510(k) number is K983362.

When did NU-GEL * WOUND DRESSING receive FDA 510(k) clearance?

NU-GEL * WOUND DRESSING received FDA 510(k) clearance on 1998-12-16, under 510(k) number K983362.

Who is the listed applicant for NU-GEL * WOUND DRESSING?

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

What is the FDA product code for NU-GEL * WOUND DRESSING?

The FDA product code for NU-GEL * WOUND DRESSING is MGQ.

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Other records listing Johnson & Johnson Medical, 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.

K001690PROTECTIV SAFETY BLOOD COLLECTION NEEDLEK982641ADVANCED NIBP MODULEK982597FIBRCOL PLUS COLLAGEN WOUND DRESSING WITH ALGINATEK974080CRITIKON SOFT BLOOD PRESSURE CUFFK980493I.V. CATHETER SYSTEMK972498OBSERVER * CENTRAL STATION

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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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