PMS PERCUTANEOUS PUNCTURE NEEDLE
K-Number: K854941 · 1986-04-16
Advertisement
Device Summary
Frequently Asked Questions
What is the PMS PERCUTANEOUS PUNCTURE NEEDLE?
PMS PERCUTANEOUS PUNCTURE NEEDLE is a medical device that received FDA 510(k) clearance on 1986-04-16. The listed applicant is Professional Medical Services. The 510(k) number is K854941.
When did PMS PERCUTANEOUS PUNCTURE NEEDLE receive FDA 510(k) clearance?
PMS PERCUTANEOUS PUNCTURE NEEDLE received FDA 510(k) clearance on 1986-04-16, under 510(k) number K854941.
Who is the listed applicant for PMS PERCUTANEOUS PUNCTURE NEEDLE?
The FDA 510(k) record lists Professional Medical Services as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PMS PERCUTANEOUS PUNCTURE NEEDLE?
The FDA product code for PMS PERCUTANEOUS PUNCTURE NEEDLE is DYB.
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 Professional Medical Services 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: DYB)
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