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FDA 510(k)

DISPOSABLE PLASTIC TRANSFUS./INFUS. ASSB

K-Number: K822354 · 1982-09-22

Decision Date1982-09-22
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE PLASTIC TRANSFUS./INFUS. ASSB is the device name listed in this FDA 510(k) record. The listed applicant is Valleylab, Inc.. It received FDA 510(k) clearance on 1982-09-22 under 510(k) number K822354. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOSABLE PLASTIC TRANSFUS./INFUS. ASSB?

DISPOSABLE PLASTIC TRANSFUS./INFUS. ASSB is a medical device that received FDA 510(k) clearance on 1982-09-22. The listed applicant is Valleylab, Inc.. The 510(k) number is K822354.

When did DISPOSABLE PLASTIC TRANSFUS./INFUS. ASSB receive FDA 510(k) clearance?

DISPOSABLE PLASTIC TRANSFUS./INFUS. ASSB received FDA 510(k) clearance on 1982-09-22, under 510(k) number K822354.

Who is the listed applicant for DISPOSABLE PLASTIC TRANSFUS./INFUS. ASSB?

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

What is the FDA product code for DISPOSABLE PLASTIC TRANSFUS./INFUS. ASSB?

The FDA product code for DISPOSABLE PLASTIC TRANSFUS./INFUS. ASSB is FPA.

Related Clinical Trials

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.

Other records listing Valleylab, Inc. 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 94 devices →

Related Devices (Code: FPA)

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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