CARRASYN FDG
K-Number: K944427 · 1994-11-29
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Device Summary
Frequently Asked Questions
What is the CARRASYN FDG?
CARRASYN FDG is a medical device that received FDA 510(k) clearance on 1994-11-29. The listed applicant is Carrington Laboratories, Inc.. The 510(k) number is K944427.
When did CARRASYN FDG receive FDA 510(k) clearance?
CARRASYN FDG received FDA 510(k) clearance on 1994-11-29, under 510(k) number K944427.
Who is the listed applicant for CARRASYN FDG?
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 CARRASYN FDG?
The FDA product code for CARRASYN FDG 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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