REFLEX(TM) CA-T CLIP APPLIER
K-Number: K873309 · 1987-11-27
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Device Summary
Frequently Asked Questions
What is the REFLEX(TM) CA-T CLIP APPLIER?
REFLEX(TM) CA-T CLIP APPLIER is a medical device that received FDA 510(k) clearance on 1987-11-27. The listed applicant is Richard-Allan Medical Ind., Inc.. The 510(k) number is K873309.
When did REFLEX(TM) CA-T CLIP APPLIER receive FDA 510(k) clearance?
REFLEX(TM) CA-T CLIP APPLIER received FDA 510(k) clearance on 1987-11-27, under 510(k) number K873309.
Who is the listed applicant for REFLEX(TM) CA-T CLIP APPLIER?
The FDA 510(k) record lists Richard-Allan Medical Ind., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for REFLEX(TM) CA-T CLIP APPLIER?
The FDA product code for REFLEX(TM) CA-T CLIP APPLIER is FZP.
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 Richard-Allan Medical Ind., 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: FZP)
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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