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FDA 510(k)

HUMAN PROTEIN S RID TEST KIT

K-Number: K951640 · 1997-04-21

ApplicantThe Binding Site, Ltd.
Decision Date1997-04-21
Product CodeGGP
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

HUMAN PROTEIN S RID TEST 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 1997-04-21 under 510(k) number K951640. The device is classified under product code GGP. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HUMAN PROTEIN S RID TEST KIT?

HUMAN PROTEIN S RID TEST KIT is a medical device that received FDA 510(k) clearance on 1997-04-21. The listed applicant is The Binding Site, Ltd.. The 510(k) number is K951640.

When did HUMAN PROTEIN S RID TEST KIT receive FDA 510(k) clearance?

HUMAN PROTEIN S RID TEST KIT received FDA 510(k) clearance on 1997-04-21, under 510(k) number K951640.

Who is the listed applicant for HUMAN PROTEIN S RID TEST 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 HUMAN PROTEIN S RID TEST KIT?

The FDA product code for HUMAN PROTEIN S RID TEST KIT is GGP.

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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.

K231290Optilite® Freelite® Kappa Free Kit, Optilite® Freelite® Lambda Free KitK090920HUMAN IGG SUBCLASS LIQUID REAGENT KITS (FOR USE ON HITACHI 911/ 912/ 917 AND MODULAR P)K083289HUMAN BETA-2 MICROGLOBULIN KITK082129HUMAN IGM LIQUID REAGENT KIT FOR USE ON THE SPAPLUS ANALYZERK081827HUMAN IGA LIQUID REAGENT KIT FOR USE ON SPAPLUSK081674BINDAZYME HUMAN ANTI-GLIADIN (MGP), IGG EIA KIT; BINDAZYME HUMAN ANTI-GLIADIN (MGP) IGA EIA KIT; (IGA OR IGG)

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Related Devices (Code: GGP)

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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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