MULTI PURPOSE SYRINGE
K-Number: K833435 · 1983-12-12
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Device Summary
Frequently Asked Questions
What is the MULTI PURPOSE SYRINGE?
MULTI PURPOSE SYRINGE is a medical device that received FDA 510(k) clearance on 1983-12-12. The listed applicant is I M, Inc.. The 510(k) number is K833435.
When did MULTI PURPOSE SYRINGE receive FDA 510(k) clearance?
MULTI PURPOSE SYRINGE received FDA 510(k) clearance on 1983-12-12, under 510(k) number K833435.
Who is the listed applicant for MULTI PURPOSE SYRINGE?
The FDA 510(k) record lists I M, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MULTI PURPOSE SYRINGE?
The FDA product code for MULTI PURPOSE 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 I M, 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: 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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