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FDA 510(k)

THERA-FLOW GRADIENT SEQUENTIAL PUMP

K-Number: K943392 · 1994-12-30

Decision Date1994-12-30
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

THERA-FLOW GRADIENT SEQUENTIAL PUMP is the device name listed in this FDA 510(k) record. The listed applicant is Meds Systems, Inc.. It received FDA 510(k) clearance on 1994-12-30 under 510(k) number K943392. The device is classified under product code JOW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THERA-FLOW GRADIENT SEQUENTIAL PUMP?

THERA-FLOW GRADIENT SEQUENTIAL PUMP is a medical device that received FDA 510(k) clearance on 1994-12-30. The listed applicant is Meds Systems, Inc.. The 510(k) number is K943392.

When did THERA-FLOW GRADIENT SEQUENTIAL PUMP receive FDA 510(k) clearance?

THERA-FLOW GRADIENT SEQUENTIAL PUMP received FDA 510(k) clearance on 1994-12-30, under 510(k) number K943392.

Who is the listed applicant for THERA-FLOW GRADIENT SEQUENTIAL PUMP?

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

What is the FDA product code for THERA-FLOW GRADIENT SEQUENTIAL PUMP?

The FDA product code for THERA-FLOW GRADIENT SEQUENTIAL PUMP is JOW.

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: JOW)

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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