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FDA 510(k)

BANDAGE ROLLS, STRETCH GAUZE ROLLS, TEXTURED GAUZE ROLLS

K-Number: K935938 · 1994-01-14

Decision Date1994-01-14
Product CodeEFQ
DecisionSubstantially Equivalent

Device Summary

BANDAGE ROLLS, STRETCH GAUZE ROLLS, TEXTURED GAUZE ROLLS is the device name listed in this FDA 510(k) record. The listed applicant is Mcneil Healthcare, Inc.. It received FDA 510(k) clearance on 1994-01-14 under 510(k) number K935938. The device is classified under product code EFQ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BANDAGE ROLLS, STRETCH GAUZE ROLLS, TEXTURED GAUZE ROLLS?

BANDAGE ROLLS, STRETCH GAUZE ROLLS, TEXTURED GAUZE ROLLS is a medical device that received FDA 510(k) clearance on 1994-01-14. The listed applicant is Mcneil Healthcare, Inc.. The 510(k) number is K935938.

When did BANDAGE ROLLS, STRETCH GAUZE ROLLS, TEXTURED GAUZE ROLLS receive FDA 510(k) clearance?

BANDAGE ROLLS, STRETCH GAUZE ROLLS, TEXTURED GAUZE ROLLS received FDA 510(k) clearance on 1994-01-14, under 510(k) number K935938.

Who is the listed applicant for BANDAGE ROLLS, STRETCH GAUZE ROLLS, TEXTURED GAUZE ROLLS?

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

What is the FDA product code for BANDAGE ROLLS, STRETCH GAUZE ROLLS, TEXTURED GAUZE ROLLS?

The FDA product code for BANDAGE ROLLS, STRETCH GAUZE ROLLS, TEXTURED GAUZE ROLLS 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 Mcneil Healthcare, 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 19 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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