CONTROL SYRINGE
K-Number: K884497 · 1988-12-12
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Device Summary
Frequently Asked Questions
What is the CONTROL SYRINGE?
CONTROL SYRINGE is a medical device that received FDA 510(k) clearance on 1988-12-12. The listed applicant is Professional Medical Services. The 510(k) number is K884497.
When did CONTROL SYRINGE receive FDA 510(k) clearance?
CONTROL SYRINGE received FDA 510(k) clearance on 1988-12-12, under 510(k) number K884497.
Who is the listed applicant for CONTROL SYRINGE?
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 CONTROL SYRINGE?
The FDA product code for CONTROL SYRINGE is FMF.
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: FMF)
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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