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FDA 510(k)

NU-BREDE PACKING AND DEBRIDEMENT SPONGE

K-Number: K921983 · 1992-09-18

Decision Date1992-09-18
Product CodeEFQ
DecisionSubstantially Equivalent

Device Summary

NU-BREDE PACKING AND DEBRIDEMENT SPONGE 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 1992-09-18 under 510(k) number K921983. The device is classified under product code EFQ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NU-BREDE PACKING AND DEBRIDEMENT SPONGE?

NU-BREDE PACKING AND DEBRIDEMENT SPONGE is a medical device that received FDA 510(k) clearance on 1992-09-18. The listed applicant is Johnson & Johnson Medical, Inc.. The 510(k) number is K921983.

When did NU-BREDE PACKING AND DEBRIDEMENT SPONGE receive FDA 510(k) clearance?

NU-BREDE PACKING AND DEBRIDEMENT SPONGE received FDA 510(k) clearance on 1992-09-18, under 510(k) number K921983.

Who is the listed applicant for NU-BREDE PACKING AND DEBRIDEMENT SPONGE?

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-BREDE PACKING AND DEBRIDEMENT SPONGE?

The FDA product code for NU-BREDE PACKING AND DEBRIDEMENT SPONGE is EFQ.

Related Clinical Trials

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.

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.

View all 53 devices →

Related Devices (Code: EFQ)

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.

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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