Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

CUSTOMED CYSTO PACK I

K-Number: K902274 · 1990-09-20

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.

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.

View all 36 devices →

Related Devices (Code: FAJ)

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.

↑