CUSTOMED ARTHROSCOPY PACK
K-Number: K902887 · 1990-09-10
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Device Summary
Frequently Asked Questions
What is the CUSTOMED ARTHROSCOPY PACK?
CUSTOMED ARTHROSCOPY PACK is a medical device that received FDA 510(k) clearance on 1990-09-10. The listed applicant is Customed, Inc.. The 510(k) number is K902887.
When did CUSTOMED ARTHROSCOPY PACK receive FDA 510(k) clearance?
CUSTOMED ARTHROSCOPY PACK received FDA 510(k) clearance on 1990-09-10, under 510(k) number K902887.
Who is the listed applicant for CUSTOMED ARTHROSCOPY PACK?
The FDA 510(k) record lists Customed, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CUSTOMED ARTHROSCOPY PACK?
The FDA product code for CUSTOMED ARTHROSCOPY PACK is LRO.
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 Customed, 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: LRO)
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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