PARENTERAL INFUSER MEDIPUMP 204
K-Number: K861001 · 1986-06-12
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Device Summary
Frequently Asked Questions
What is the PARENTERAL INFUSER MEDIPUMP 204?
PARENTERAL INFUSER MEDIPUMP 204 is a medical device that received FDA 510(k) clearance on 1986-06-12. The listed applicant is Medix Medical Electronics (U.S.A.), Inc.. The 510(k) number is K861001.
When did PARENTERAL INFUSER MEDIPUMP 204 receive FDA 510(k) clearance?
PARENTERAL INFUSER MEDIPUMP 204 received FDA 510(k) clearance on 1986-06-12, under 510(k) number K861001.
Who is the listed applicant for PARENTERAL INFUSER MEDIPUMP 204?
The FDA 510(k) record lists Medix Medical Electronics (U.S.A.), Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PARENTERAL INFUSER MEDIPUMP 204?
The FDA product code for PARENTERAL INFUSER MEDIPUMP 204 is FRN.
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 Medix Medical Electronics (U.S.A.), Inc. 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: FRN)
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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