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FDA 510(k)

PFEIFFER PUMP

K-Number: K851525 · 1985-08-08

ApplicantIng. Erich Pfeiffer GmbH & Co. Kg.
Decision Date1985-08-08
Product CodeCCQ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PFEIFFER PUMP is the device name listed in this FDA 510(k) record. The listed applicant is Ing. Erich Pfeiffer GmbH & Co. Kg.. It received FDA 510(k) clearance on 1985-08-08 under 510(k) number K851525. The device is classified under product code CCQ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PFEIFFER PUMP?

PFEIFFER PUMP is a medical device that received FDA 510(k) clearance on 1985-08-08. The listed applicant is Ing. Erich Pfeiffer GmbH & Co. Kg.. The 510(k) number is K851525.

When did PFEIFFER PUMP receive FDA 510(k) clearance?

PFEIFFER PUMP received FDA 510(k) clearance on 1985-08-08, under 510(k) number K851525.

Who is the listed applicant for PFEIFFER PUMP?

The FDA 510(k) record lists Ing. Erich Pfeiffer GmbH & Co. Kg. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PFEIFFER PUMP?

The FDA product code for PFEIFFER PUMP is CCQ.

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Related Devices (Code: CCQ)

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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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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