MULTIPLE STERILE GAUZE BANDAGE ROLLS, VARI SIZES
K-Number: K915821 · 1992-05-29
Advertisement
Device Summary
Frequently Asked Questions
What is the MULTIPLE STERILE GAUZE BANDAGE ROLLS, VARI SIZES?
MULTIPLE STERILE GAUZE BANDAGE ROLLS, VARI SIZES is a medical device that received FDA 510(k) clearance on 1992-05-29. The listed applicant is Kerma Medical Products, Inc.. The 510(k) number is K915821.
When did MULTIPLE STERILE GAUZE BANDAGE ROLLS, VARI SIZES receive FDA 510(k) clearance?
MULTIPLE STERILE GAUZE BANDAGE ROLLS, VARI SIZES received FDA 510(k) clearance on 1992-05-29, under 510(k) number K915821.
Who is the listed applicant for MULTIPLE STERILE GAUZE BANDAGE ROLLS, VARI SIZES?
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 MULTIPLE STERILE GAUZE BANDAGE ROLLS, VARI SIZES?
The FDA product code for MULTIPLE STERILE GAUZE BANDAGE ROLLS, VARI SIZES 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.
Advertisement