REFLEX(TM) CLIP APPLIER
K-Number: K862404 · 1986-07-23
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Device Summary
Frequently Asked Questions
What is the REFLEX(TM) CLIP APPLIER?
REFLEX(TM) CLIP APPLIER is a medical device that received FDA 510(k) clearance on 1986-07-23. The listed applicant is Richard-Allan Medical Ind., Inc.. The 510(k) number is K862404.
When did REFLEX(TM) CLIP APPLIER receive FDA 510(k) clearance?
REFLEX(TM) CLIP APPLIER received FDA 510(k) clearance on 1986-07-23, under 510(k) number K862404.
Who is the listed applicant for REFLEX(TM) 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) CLIP APPLIER?
The FDA product code for REFLEX(TM) 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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