PROVIDER PUMP SET W/INFUSION CARTRIDGE
K-Number: K934513 · 1994-07-29
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Device Summary
Frequently Asked Questions
What is the PROVIDER PUMP SET W/INFUSION CARTRIDGE?
PROVIDER PUMP SET W/INFUSION CARTRIDGE is a medical device that received FDA 510(k) clearance on 1994-07-29. The listed applicant is Abbott Laboratories. The 510(k) number is K934513.
When did PROVIDER PUMP SET W/INFUSION CARTRIDGE receive FDA 510(k) clearance?
PROVIDER PUMP SET W/INFUSION CARTRIDGE received FDA 510(k) clearance on 1994-07-29, under 510(k) number K934513.
Who is the listed applicant for PROVIDER PUMP SET W/INFUSION CARTRIDGE?
The FDA 510(k) record lists Abbott Laboratories as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PROVIDER PUMP SET W/INFUSION CARTRIDGE?
The FDA product code for PROVIDER PUMP SET W/INFUSION CARTRIDGE 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 Abbott Laboratories 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: 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
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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