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FDA 510(k)

VOLUMETRIC PUMP SOLUTION SET W/INTEGRAL AIRWAY

K-Number: K893646 · 1989-12-06

Decision Date1989-12-06
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VOLUMETRIC PUMP SOLUTION SET W/INTEGRAL AIRWAY is the device name listed in this FDA 510(k) record. The listed applicant is Baxter Healthcare Corp. It received FDA 510(k) clearance on 1989-12-06 under 510(k) number K893646. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VOLUMETRIC PUMP SOLUTION SET W/INTEGRAL AIRWAY?

VOLUMETRIC PUMP SOLUTION SET W/INTEGRAL AIRWAY is a medical device that received FDA 510(k) clearance on 1989-12-06. The listed applicant is Baxter Healthcare Corp. The 510(k) number is K893646.

When did VOLUMETRIC PUMP SOLUTION SET W/INTEGRAL AIRWAY receive FDA 510(k) clearance?

VOLUMETRIC PUMP SOLUTION SET W/INTEGRAL AIRWAY received FDA 510(k) clearance on 1989-12-06, under 510(k) number K893646.

Who is the listed applicant for VOLUMETRIC PUMP SOLUTION SET W/INTEGRAL AIRWAY?

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 VOLUMETRIC PUMP SOLUTION SET W/INTEGRAL AIRWAY?

The FDA product code for VOLUMETRIC PUMP SOLUTION SET W/INTEGRAL AIRWAY is FPA.

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.

View all 504 devices →

Related Devices (Code: FPA)

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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