FLO-GARD 6300 DUAL CHANNEL VOLUME INFUSION PUMP
K-Number: K891289 · 1990-02-02
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Device Summary
Frequently Asked Questions
What is the FLO-GARD 6300 DUAL CHANNEL VOLUME INFUSION PUMP?
FLO-GARD 6300 DUAL CHANNEL VOLUME INFUSION PUMP is a medical device that received FDA 510(k) clearance on 1990-02-02. The listed applicant is Baxter Healthcare Corp. The 510(k) number is K891289.
When did FLO-GARD 6300 DUAL CHANNEL VOLUME INFUSION PUMP receive FDA 510(k) clearance?
FLO-GARD 6300 DUAL CHANNEL VOLUME INFUSION PUMP received FDA 510(k) clearance on 1990-02-02, under 510(k) number K891289.
Who is the listed applicant for FLO-GARD 6300 DUAL CHANNEL VOLUME INFUSION PUMP?
The FDA 510(k) record lists Baxter Healthcare Corp as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FLO-GARD 6300 DUAL CHANNEL VOLUME INFUSION PUMP?
The FDA product code for FLO-GARD 6300 DUAL CHANNEL VOLUME INFUSION 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.
Other records listing Baxter Healthcare Corp 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.
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
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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