Decision Date1990-09-20
Product CodeFAJ
Advisory CommitteeGU
DecisionUnknown
Device Summary
CUSTOMED CYSTO PACK I is the device name listed in this FDA 510(k) record. The listed applicant is Customed, Inc.. It received FDA 510(k) clearance on 1990-09-20 under 510(k) number K902274. The device is classified under product code FAJ. It was reviewed by the GU advisory panel. FDA Decision: Unknown.
Frequently Asked Questions
What is the CUSTOMED CYSTO PACK I?
CUSTOMED CYSTO PACK I is a medical device that received FDA 510(k) clearance on 1990-09-20. The listed applicant is Customed, Inc.. The 510(k) number is K902274.
When did CUSTOMED CYSTO PACK I receive FDA 510(k) clearance?
CUSTOMED CYSTO PACK I received FDA 510(k) clearance on 1990-09-20, under 510(k) number K902274.
Who is the listed applicant for CUSTOMED CYSTO PACK I?
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 CYSTO PACK I?
The FDA product code for CUSTOMED CYSTO PACK I is FAJ.
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Official Source
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