SURGIPUMP
K-Number: K935763 · 1994-04-21
Advertisement
Device Summary
Frequently Asked Questions
What is the SURGIPUMP?
SURGIPUMP is a medical device that received FDA 510(k) clearance on 1994-04-21. The listed applicant is W.O.M. World of Medicine GmbH. The 510(k) number is K935763.
When did SURGIPUMP receive FDA 510(k) clearance?
SURGIPUMP received FDA 510(k) clearance on 1994-04-21, under 510(k) number K935763.
Who is the listed applicant for SURGIPUMP?
The FDA 510(k) record lists W.O.M. World of Medicine GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SURGIPUMP?
The FDA product code for SURGIPUMP 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 W.O.M. World of Medicine GmbH 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.
Advertisement