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FDA 510(k)

BARD AMBU PUMP SPIK TUB SET PACRET PROVID PUMP SET

K-Number: K925058 · 1993-08-03

Decision Date1993-08-03
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BARD AMBU PUMP SPIK TUB SET PACRET PROVID PUMP SET is the device name listed in this FDA 510(k) record. The listed applicant is C.R. Bard, Inc.. It received FDA 510(k) clearance on 1993-08-03 under 510(k) number K925058. 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 BARD AMBU PUMP SPIK TUB SET PACRET PROVID PUMP SET?

BARD AMBU PUMP SPIK TUB SET PACRET PROVID PUMP SET is a medical device that received FDA 510(k) clearance on 1993-08-03. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K925058.

When did BARD AMBU PUMP SPIK TUB SET PACRET PROVID PUMP SET receive FDA 510(k) clearance?

BARD AMBU PUMP SPIK TUB SET PACRET PROVID PUMP SET received FDA 510(k) clearance on 1993-08-03, under 510(k) number K925058.

Who is the listed applicant for BARD AMBU PUMP SPIK TUB SET PACRET PROVID PUMP SET?

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

What is the FDA product code for BARD AMBU PUMP SPIK TUB SET PACRET PROVID PUMP SET?

The FDA product code for BARD AMBU PUMP SPIK TUB SET PACRET PROVID PUMP 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 C.R. Bard, 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 616 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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