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FDA 510(k)

REAGENT, PARTIAL THROMBOPLASTIN

K-Number: K760499 · 1976-10-29

ApplicantHyland Therapeutic Div., Travenol Laboratories
Decision Date1976-10-29
Product Code
DecisionSubstantially Equivalent

Device Summary

REAGENT, PARTIAL THROMBOPLASTIN is the device name listed in this FDA 510(k) record. The listed applicant is Hyland Therapeutic Div., Travenol Laboratories. It received FDA 510(k) clearance on 1976-10-29 under 510(k) number K760499. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REAGENT, PARTIAL THROMBOPLASTIN?

REAGENT, PARTIAL THROMBOPLASTIN is a medical device that received FDA 510(k) clearance on 1976-10-29. The listed applicant is Hyland Therapeutic Div., Travenol Laboratories. The 510(k) number is K760499.

When did REAGENT, PARTIAL THROMBOPLASTIN receive FDA 510(k) clearance?

REAGENT, PARTIAL THROMBOPLASTIN received FDA 510(k) clearance on 1976-10-29, under 510(k) number K760499.

Who is the listed applicant for REAGENT, PARTIAL THROMBOPLASTIN?

The FDA 510(k) record lists Hyland Therapeutic Div., Travenol Laboratories as the applicant. This does not by itself establish the device manufacturer.

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Other records listing Hyland Therapeutic Div., Travenol Laboratories 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.

K820835ALUMINA SILICA-ACTIVATED PARTIAL THROMK820192HAEMOPHILUS INFLUENZAE TYPE B ANTISERUMK812220NEPHELOMETRIC SOLID TURBIDITY STANDARDK810078Q-PAK THERAPEUTIC DRUG MONIT. CONTROL SK810077OMEGA THERAPEUTIC DRUG MONIT. CONTROL S.K802610ALERT A,HDL-APOLIPOROTEIN A, TEST KIT

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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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