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FDA 510(k)

BURN DRESSING

K-Number: K923846 · 1992-09-11

ApplicantMedical Action Industries, Inc.
Decision Date1992-09-11
Product CodeNAB
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

BURN DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Medical Action Industries, Inc.. It received FDA 510(k) clearance on 1992-09-11 under 510(k) number K923846. The device is classified under product code NAB. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BURN DRESSING?

BURN DRESSING is a medical device that received FDA 510(k) clearance on 1992-09-11. The listed applicant is Medical Action Industries, Inc.. The 510(k) number is K923846.

When did BURN DRESSING receive FDA 510(k) clearance?

BURN DRESSING received FDA 510(k) clearance on 1992-09-11, under 510(k) number K923846.

Who is the listed applicant for BURN DRESSING?

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

What is the FDA product code for BURN DRESSING?

The FDA product code for BURN DRESSING is NAB.

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Other records listing Medical Action Industries, 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.

K042526DRAPE, SURGICAL, X-RAY ELEMENT, MODELS NON STERILE 6120-00, STERILE 704-B, NON STERILE 6124-00X, STERILE 704-BXK042527SPATULA, CERVICAL, CYTOLOGICAL, MODEL 22-9107K022948VAGINAL SPECULUM, MODEL 5555S, 5555M, OR 5555LK946019SURGICLA INSTRUMENT KITK884826GAUZE SPONGEK810685SUTURE REMOVAL KIT

View all 8 devices →

Related Devices (Code: NAB)

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.

K946015IVALON EXTERNAL SPONGEIvalonK940755ISOLYER (4X4, 8PLY)Isolyer Co.K931610OMNISORB II, NONWOVEN SPONGE, STERILE AND NONOmni Mfg., Inc.K925590MULTI-TRAUMA DRESSINGGam Industries, Inc.K926072K-BAND AND K-CREPEParema , Ltd.K915591STERILE GAUZE PADSEagle Medical, Inc.

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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