FLUID DISPENSING SYSTEM
K-Number: K761158 · 1977-01-26
Advertisement
Device Summary
Frequently Asked Questions
What is the FLUID DISPENSING SYSTEM?
FLUID DISPENSING SYSTEM is a medical device that received FDA 510(k) clearance on 1977-01-26. The listed applicant is Pharmaseal Div., Baxter Healthcare Corp.. The 510(k) number is K761158.
When did FLUID DISPENSING SYSTEM receive FDA 510(k) clearance?
FLUID DISPENSING SYSTEM received FDA 510(k) clearance on 1977-01-26, under 510(k) number K761158.
Who is the listed applicant for FLUID DISPENSING SYSTEM?
The FDA 510(k) record lists Pharmaseal Div., Baxter Healthcare Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FLUID DISPENSING SYSTEM?
The FDA product code for FLUID DISPENSING SYSTEM is FMF.
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 Pharmaseal Div., 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: FMF)
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.
Advertisement