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FDA 510(k)

RIVER PUMP

K-Number: K932895 · 1994-03-31

ApplicantRiver Medical, Inc.
Decision Date1994-03-31
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

RIVER PUMP is the device name listed in this FDA 510(k) record. The listed applicant is River Medical, Inc.. It received FDA 510(k) clearance on 1994-03-31 under 510(k) number K932895. 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 RIVER PUMP?

RIVER PUMP is a medical device that received FDA 510(k) clearance on 1994-03-31. The listed applicant is River Medical, Inc.. The 510(k) number is K932895.

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

RIVER PUMP received FDA 510(k) clearance on 1994-03-31, under 510(k) number K932895.

Who is the listed applicant for RIVER PUMP?

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

What is the FDA product code for RIVER PUMP?

The FDA product code for RIVER PUMP is FRN.

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Other records listing River Medical, 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.

K023174DISPOSABLE TEMPORARY PACING WIREK944351SMARTDOSE IV PREFILLED INFUSION CONTAINERK944352SMARTDOSE III INFUSION CONTAINERK945298SMARTFLOW I ADMINISTRATION SETK943692SMART DOSE(TM)K933335RIVER VIAL ADAPTER

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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.

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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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