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FDA 510(k)

SPECIALTY SET MODEL IV7A01

K-Number: K830891 · 1983-04-14

Decision Date1983-04-14
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SPECIALTY SET MODEL IV7A01 is the device name listed in this FDA 510(k) record. The listed applicant is Valleylab, Inc.. It received FDA 510(k) clearance on 1983-04-14 under 510(k) number K830891. 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 SPECIALTY SET MODEL IV7A01?

SPECIALTY SET MODEL IV7A01 is a medical device that received FDA 510(k) clearance on 1983-04-14. The listed applicant is Valleylab, Inc.. The 510(k) number is K830891.

When did SPECIALTY SET MODEL IV7A01 receive FDA 510(k) clearance?

SPECIALTY SET MODEL IV7A01 received FDA 510(k) clearance on 1983-04-14, under 510(k) number K830891.

Who is the listed applicant for SPECIALTY SET MODEL IV7A01?

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 SPECIALTY SET MODEL IV7A01?

The FDA product code for SPECIALTY SET MODEL IV7A01 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.

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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

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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