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FDA 510(k)

NU-GEL ISLAND WOUND DRESSING

K-Number: K932336 · 1994-02-09

ApplicantJohnson & Johnson Medical, Inc.
Decision Date1994-02-09
Product CodeNAE
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

NU-GEL ISLAND 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 1994-02-09 under 510(k) number K932336. The device is classified under product code NAE. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NU-GEL ISLAND WOUND DRESSING?

NU-GEL ISLAND WOUND DRESSING is a medical device that received FDA 510(k) clearance on 1994-02-09. The listed applicant is Johnson & Johnson Medical, Inc.. The 510(k) number is K932336.

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

NU-GEL ISLAND WOUND DRESSING received FDA 510(k) clearance on 1994-02-09, under 510(k) number K932336.

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

The FDA product code for NU-GEL ISLAND WOUND DRESSING is NAE.

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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 MODULEK983362NU-GEL * WOUND DRESSINGK982597FIBRCOL PLUS COLLAGEN WOUND DRESSING WITH ALGINATEK974080CRITIKON SOFT BLOOD PRESSURE CUFFK980493I.V. CATHETER SYSTEM

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Related Devices (Code: NAE)

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.

K083721MODIFICATION TO ZENIEVARiver'S Edge Pharmaceuticals, LLCK082865MODIFICATION TO ZENIEVAGorbec Pharmaceutical Services, Inc.K073246ZENIEVAGorbec Pharmaceutical Services, Inc.K992094GILTECH PLUS HYDROGEL SKIN DRESSINGGiltech Plus, Inc.K991061DERMAPHYLYX CALCIUM ALGINATE WOUND DRESSINGDermaphylyx, Inc.K972646AD-HEAL HYDROGEL DRESSING, VARIOUS SIZESLudlow Technical Products

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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