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FDA 510(k)

SOLUTION ADMINISTRATION SET

K-Number: K921429 · 1992-12-17

Decision Date1992-12-17
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SOLUTION ADMINISTRATION SET is the device name listed in this FDA 510(k) record. The listed applicant is Sierra Medical Devices. It received FDA 510(k) clearance on 1992-12-17 under 510(k) number K921429. 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 SOLUTION ADMINISTRATION SET?

SOLUTION ADMINISTRATION SET is a medical device that received FDA 510(k) clearance on 1992-12-17. The listed applicant is Sierra Medical Devices. The 510(k) number is K921429.

When did SOLUTION ADMINISTRATION SET receive FDA 510(k) clearance?

SOLUTION ADMINISTRATION SET received FDA 510(k) clearance on 1992-12-17, under 510(k) number K921429.

Who is the listed applicant for SOLUTION ADMINISTRATION SET?

The FDA 510(k) record lists Sierra Medical Devices as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SOLUTION ADMINISTRATION SET?

The FDA product code for SOLUTION ADMINISTRATION SET 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 Sierra Medical Devices 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.

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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