STERILE GAUZE PK STRIPS SAT W/CARR GEL WOUND DRESS
K-Number: K915002 · 1992-01-31
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Device Summary
Frequently Asked Questions
What is the STERILE GAUZE PK STRIPS SAT W/CARR GEL WOUND DRESS?
STERILE GAUZE PK STRIPS SAT W/CARR GEL WOUND DRESS is a medical device that received FDA 510(k) clearance on 1992-01-31. The listed applicant is Carrington Laboratories, Inc.. The 510(k) number is K915002.
When did STERILE GAUZE PK STRIPS SAT W/CARR GEL WOUND DRESS receive FDA 510(k) clearance?
STERILE GAUZE PK STRIPS SAT W/CARR GEL WOUND DRESS received FDA 510(k) clearance on 1992-01-31, under 510(k) number K915002.
Who is the listed applicant for STERILE GAUZE PK STRIPS SAT W/CARR GEL WOUND DRESS?
The FDA 510(k) record lists Carrington Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for STERILE GAUZE PK STRIPS SAT W/CARR GEL WOUND DRESS?
The FDA product code for STERILE GAUZE PK STRIPS SAT W/CARR GEL WOUND DRESS is MGQ.
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 Carrington Laboratories, 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: MGQ)
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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