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FDA 510(k)

SYRINGE DRIVER 209

K-Number: K813562 · 1982-02-01

ApplicantMedix Medical Electronics (U.S.A.), Inc.
Decision Date1982-02-01
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SYRINGE DRIVER 209 is the device name listed in this FDA 510(k) record. The listed applicant is Medix Medical Electronics (U.S.A.), Inc.. It received FDA 510(k) clearance on 1982-02-01 under 510(k) number K813562. 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 SYRINGE DRIVER 209?

SYRINGE DRIVER 209 is a medical device that received FDA 510(k) clearance on 1982-02-01. The listed applicant is Medix Medical Electronics (U.S.A.), Inc.. The 510(k) number is K813562.

When did SYRINGE DRIVER 209 receive FDA 510(k) clearance?

SYRINGE DRIVER 209 received FDA 510(k) clearance on 1982-02-01, under 510(k) number K813562.

Who is the listed applicant for SYRINGE DRIVER 209?

The FDA 510(k) record lists Medix Medical Electronics (U.S.A.), Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SYRINGE DRIVER 209?

The FDA product code for SYRINGE DRIVER 209 is FRN.

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Other records listing Medix Medical Electronics (U.S.A.), Inc. as applicant

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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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