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FDA 510(k)

OFFENBACK REVERSIBLE BARIUM PUMP

K-Number: K803183 · 1981-06-09

Decision Date1981-06-09
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

OFFENBACK REVERSIBLE BARIUM PUMP is the device name listed in this FDA 510(k) record. The listed applicant is The Offenback Co.. It received FDA 510(k) clearance on 1981-06-09 under 510(k) number K803183. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OFFENBACK REVERSIBLE BARIUM PUMP?

OFFENBACK REVERSIBLE BARIUM PUMP is a medical device that received FDA 510(k) clearance on 1981-06-09. The listed applicant is The Offenback Co.. The 510(k) number is K803183.

When did OFFENBACK REVERSIBLE BARIUM PUMP receive FDA 510(k) clearance?

OFFENBACK REVERSIBLE BARIUM PUMP received FDA 510(k) clearance on 1981-06-09, under 510(k) number K803183.

Who is the listed applicant for OFFENBACK REVERSIBLE BARIUM PUMP?

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

What is the FDA product code for OFFENBACK REVERSIBLE BARIUM PUMP?

The FDA product code for OFFENBACK REVERSIBLE BARIUM PUMP is FRN.

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.

Related Devices (Code: FRN)

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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