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FDA 510(k)

MODEL 113 TREONIC IP3 DIGITAL SYRINGE PU

K-Number: K790945 · 1979-06-01

ApplicantVickers America Medical Corp.
Decision Date1979-06-01
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MODEL 113 TREONIC IP3 DIGITAL SYRINGE PU is the device name listed in this FDA 510(k) record. The listed applicant is Vickers America Medical Corp.. It received FDA 510(k) clearance on 1979-06-01 under 510(k) number K790945. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 113 TREONIC IP3 DIGITAL SYRINGE PU?

MODEL 113 TREONIC IP3 DIGITAL SYRINGE PU is a medical device that received FDA 510(k) clearance on 1979-06-01. The listed applicant is Vickers America Medical Corp.. The 510(k) number is K790945.

When did MODEL 113 TREONIC IP3 DIGITAL SYRINGE PU receive FDA 510(k) clearance?

MODEL 113 TREONIC IP3 DIGITAL SYRINGE PU received FDA 510(k) clearance on 1979-06-01, under 510(k) number K790945.

Who is the listed applicant for MODEL 113 TREONIC IP3 DIGITAL SYRINGE PU?

The FDA 510(k) record lists Vickers America Medical Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODEL 113 TREONIC IP3 DIGITAL SYRINGE PU?

The FDA product code for MODEL 113 TREONIC IP3 DIGITAL SYRINGE PU is FRN.

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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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