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FDA 510(k)

CONFORMING BANDAGE

K-Number: K912692 · 1991-10-04

ApplicantUlti-Med Intl., Inc.
Decision Date1991-10-04
Product CodeNAB
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CONFORMING BANDAGE is the device name listed in this FDA 510(k) record. The listed applicant is Ulti-Med Intl., Inc.. It received FDA 510(k) clearance on 1991-10-04 under 510(k) number K912692. 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 CONFORMING BANDAGE?

CONFORMING BANDAGE is a medical device that received FDA 510(k) clearance on 1991-10-04. The listed applicant is Ulti-Med Intl., Inc.. The 510(k) number is K912692.

When did CONFORMING BANDAGE receive FDA 510(k) clearance?

CONFORMING BANDAGE received FDA 510(k) clearance on 1991-10-04, under 510(k) number K912692.

Who is the listed applicant for CONFORMING BANDAGE?

The FDA 510(k) record lists Ulti-Med Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CONFORMING BANDAGE?

The FDA product code for CONFORMING BANDAGE is NAB.

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Other records listing Ulti-Med Intl., 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.

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Related Devices (Code: NAB)

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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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