STERILE BANDAGE, GAUZE, FINE MESH, 3X8 INCHES
K-Number: K914937 · 1991-12-04
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Device Summary
Frequently Asked Questions
What is the STERILE BANDAGE, GAUZE, FINE MESH, 3X8 INCHES?
STERILE BANDAGE, GAUZE, FINE MESH, 3X8 INCHES is a medical device that received FDA 510(k) clearance on 1991-12-04. The listed applicant is Kerma Medical Products, Inc.. The 510(k) number is K914937.
When did STERILE BANDAGE, GAUZE, FINE MESH, 3X8 INCHES receive FDA 510(k) clearance?
STERILE BANDAGE, GAUZE, FINE MESH, 3X8 INCHES received FDA 510(k) clearance on 1991-12-04, under 510(k) number K914937.
Who is the listed applicant for STERILE BANDAGE, GAUZE, FINE MESH, 3X8 INCHES?
The FDA 510(k) record lists Kerma Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for STERILE BANDAGE, GAUZE, FINE MESH, 3X8 INCHES?
The FDA product code for STERILE BANDAGE, GAUZE, FINE MESH, 3X8 INCHES is NAB.
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 Kerma Medical Products, 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.
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.
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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