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FDA 510(k)

C3C AND C4 RID KITS

K-Number: K902382 · 1990-09-07

Decision Date1990-09-07
Product CodeCZW
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

C3C AND C4 RID KITS is the device name listed in this FDA 510(k) record. The listed applicant is The Binding Site, Ltd.. It received FDA 510(k) clearance on 1990-09-07 under 510(k) number K902382. The device is classified under product code CZW. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the C3C AND C4 RID KITS?

C3C AND C4 RID KITS is a medical device that received FDA 510(k) clearance on 1990-09-07. The listed applicant is The Binding Site, Ltd.. The 510(k) number is K902382.

When did C3C AND C4 RID KITS receive FDA 510(k) clearance?

C3C AND C4 RID KITS received FDA 510(k) clearance on 1990-09-07, under 510(k) number K902382.

Who is the listed applicant for C3C AND C4 RID KITS?

The FDA 510(k) record lists The Binding Site, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for C3C AND C4 RID KITS?

The FDA product code for C3C AND C4 RID KITS is CZW.

Other records listing The Binding Site, Ltd. 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 115 devices →

Related Devices (Code: CZW)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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