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FDA 510(k)

COVER-ROLL STRETCH

K-Number: K823879 · 1983-03-09

ApplicantBeiersdorf, Inc.
Decision Date1983-03-09
Product CodeNAB
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

COVER-ROLL STRETCH is the device name listed in this FDA 510(k) record. The listed applicant is Beiersdorf, Inc.. It received FDA 510(k) clearance on 1983-03-09 under 510(k) number K823879. 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 COVER-ROLL STRETCH?

COVER-ROLL STRETCH is a medical device that received FDA 510(k) clearance on 1983-03-09. The listed applicant is Beiersdorf, Inc.. The 510(k) number is K823879.

When did COVER-ROLL STRETCH receive FDA 510(k) clearance?

COVER-ROLL STRETCH received FDA 510(k) clearance on 1983-03-09, under 510(k) number K823879.

Who is the listed applicant for COVER-ROLL STRETCH?

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

What is the FDA product code for COVER-ROLL STRETCH?

The FDA product code for COVER-ROLL STRETCH is NAB.

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Other records listing Beiersdorf, Inc. as applicant

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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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