JMS INFUSION SET
K-Number: K860242 · 1986-02-13
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Device Summary
Frequently Asked Questions
What is the JMS INFUSION SET?
JMS INFUSION SET is a medical device that received FDA 510(k) clearance on 1986-02-13. The listed applicant is Sturbridge Medical. The 510(k) number is K860242.
When did JMS INFUSION SET receive FDA 510(k) clearance?
JMS INFUSION SET received FDA 510(k) clearance on 1986-02-13, under 510(k) number K860242.
Who is the listed applicant for JMS INFUSION SET?
The FDA 510(k) record lists Sturbridge Medical as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for JMS INFUSION SET?
The FDA product code for JMS 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 Sturbridge Medical 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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