DEXON S, DEXON PLUS, AND DEXON II POLYCOLIC ACID
K-Number: K930588 · 1994-01-07
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Device Summary
Frequently Asked Questions
What is the DEXON S, DEXON PLUS, AND DEXON II POLYCOLIC ACID?
DEXON S, DEXON PLUS, AND DEXON II POLYCOLIC ACID is a medical device that received FDA 510(k) clearance on 1994-01-07. The listed applicant is Davis & Geck, Inc.. The 510(k) number is K930588.
When did DEXON S, DEXON PLUS, AND DEXON II POLYCOLIC ACID receive FDA 510(k) clearance?
DEXON S, DEXON PLUS, AND DEXON II POLYCOLIC ACID received FDA 510(k) clearance on 1994-01-07, under 510(k) number K930588.
Who is the listed applicant for DEXON S, DEXON PLUS, AND DEXON II POLYCOLIC ACID?
The FDA 510(k) record lists Davis & Geck, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DEXON S, DEXON PLUS, AND DEXON II POLYCOLIC ACID?
The FDA product code for DEXON S, DEXON PLUS, AND DEXON II POLYCOLIC ACID is GAM.
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 Davis & Geck, 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: GAM)
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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