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FDA 510(k)

C1 RID KIT

K-Number: K914388 · 1991-10-28

Decision Date1991-10-28
Product CodeDAK
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

C1 RID KIT 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 1991-10-28 under 510(k) number K914388. The device is classified under product code DAK. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the C1 RID KIT?

C1 RID KIT is a medical device that received FDA 510(k) clearance on 1991-10-28. The listed applicant is The Binding Site, Ltd.. The 510(k) number is K914388.

When did C1 RID KIT receive FDA 510(k) clearance?

C1 RID KIT received FDA 510(k) clearance on 1991-10-28, under 510(k) number K914388.

Who is the listed applicant for C1 RID KIT?

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 C1 RID KIT?

The FDA product code for C1 RID KIT is DAK.

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: DAK)

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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