BAXTER ANGIOSCOPY PUMP TUBING SET (MODEL NL)
K-Number: K905189 · 1991-01-30
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Device Summary
Frequently Asked Questions
What is the BAXTER ANGIOSCOPY PUMP TUBING SET (MODEL NL)?
BAXTER ANGIOSCOPY PUMP TUBING SET (MODEL NL) is a medical device that received FDA 510(k) clearance on 1991-01-30. The listed applicant is Baxter Healthcare Corp. The 510(k) number is K905189.
When did BAXTER ANGIOSCOPY PUMP TUBING SET (MODEL NL) receive FDA 510(k) clearance?
BAXTER ANGIOSCOPY PUMP TUBING SET (MODEL NL) received FDA 510(k) clearance on 1991-01-30, under 510(k) number K905189.
Who is the listed applicant for BAXTER ANGIOSCOPY PUMP TUBING SET (MODEL NL)?
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 BAXTER ANGIOSCOPY PUMP TUBING SET (MODEL NL)?
The FDA product code for BAXTER ANGIOSCOPY PUMP TUBING SET (MODEL NL) is DQI.
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: DQI)
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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