FDA 510(k)

STRETCH BANDAGE

K-Number: K852858 · 1985-07-26

Decision Date1985-07-26

Product Code

DecisionSubstantially Equivalent

Device Summary

STRETCH BANDAGE is the device name listed in this FDA 510(k) record. The listed applicant is Cornelia Damsky, Inc.. It received FDA 510(k) clearance on 1985-07-26 under 510(k) number K852858. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STRETCH BANDAGE?

STRETCH BANDAGE is a medical device that received FDA 510(k) clearance on 1985-07-26. The listed applicant is Cornelia Damsky, Inc.. The 510(k) number is K852858.

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

STRETCH BANDAGE received FDA 510(k) clearance on 1985-07-26, under 510(k) number K852858.

Who is the listed applicant for STRETCH BANDAGE?

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

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.

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Other records listing Cornelia Damsky, Inc. as applicant

K001322PERFORMER 30 HPS K946321BIOSTRIP STERILE WOUND CLOSURE STRIP K8528574 X 4' GAUZE PAD

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.