MESULIN INSULIN INFUSION SET
K-Number: K833398 · 1984-03-06
Advertisement
Device Summary
Frequently Asked Questions
What is the MESULIN INSULIN INFUSION SET?
MESULIN INSULIN INFUSION SET is a medical device that received FDA 510(k) clearance on 1984-03-06. The listed applicant is Molnlycke A/S Hospital Products. The 510(k) number is K833398.
When did MESULIN INSULIN INFUSION SET receive FDA 510(k) clearance?
MESULIN INSULIN INFUSION SET received FDA 510(k) clearance on 1984-03-06, under 510(k) number K833398.
Who is the listed applicant for MESULIN INSULIN INFUSION SET?
The FDA 510(k) record lists Molnlycke A/S Hospital Products as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MESULIN INSULIN INFUSION SET?
The FDA product code for MESULIN INSULIN INFUSION SET 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 Molnlycke A/S Hospital Products 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.
Advertisement