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FDA 510(k)

IMMUNOGLOBULINS G, A & M LIGHT CHAIN SPECIFIC

K-Number: K924767 · 1993-02-23

ApplicantThe Binding Site, Ltd.
Decision Date1993-02-23
Product CodeCFF
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

IMMUNOGLOBULINS G, A & M LIGHT CHAIN SPECIFIC 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 1993-02-23 under 510(k) number K924767. The device is classified under product code CFF. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IMMUNOGLOBULINS G, A & M LIGHT CHAIN SPECIFIC?

IMMUNOGLOBULINS G, A & M LIGHT CHAIN SPECIFIC is a medical device that received FDA 510(k) clearance on 1993-02-23. The listed applicant is The Binding Site, Ltd.. The 510(k) number is K924767.

When did IMMUNOGLOBULINS G, A & M LIGHT CHAIN SPECIFIC receive FDA 510(k) clearance?

IMMUNOGLOBULINS G, A & M LIGHT CHAIN SPECIFIC received FDA 510(k) clearance on 1993-02-23, under 510(k) number K924767.

Who is the listed applicant for IMMUNOGLOBULINS G, A & M LIGHT CHAIN SPECIFIC?

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 IMMUNOGLOBULINS G, A & M LIGHT CHAIN SPECIFIC?

The FDA product code for IMMUNOGLOBULINS G, A & M LIGHT CHAIN SPECIFIC is CFF.

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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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