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FDA 510(k)

20CC GLASS CONTROL SYRINGE

K-Number: K813175 · 1981-11-27

ApplicantAbco Dealers, Inc.
Decision Date1981-11-27
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

20CC GLASS CONTROL SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is Abco Dealers, Inc.. It received FDA 510(k) clearance on 1981-11-27 under 510(k) number K813175. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 20CC GLASS CONTROL SYRINGE?

20CC GLASS CONTROL SYRINGE is a medical device that received FDA 510(k) clearance on 1981-11-27. The listed applicant is Abco Dealers, Inc.. The 510(k) number is K813175.

When did 20CC GLASS CONTROL SYRINGE receive FDA 510(k) clearance?

20CC GLASS CONTROL SYRINGE received FDA 510(k) clearance on 1981-11-27, under 510(k) number K813175.

Who is the listed applicant for 20CC GLASS CONTROL SYRINGE?

The FDA 510(k) record lists Abco Dealers, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 20CC GLASS CONTROL SYRINGE?

The FDA product code for 20CC GLASS CONTROL SYRINGE is FMF.

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Other records listing Abco Dealers, Inc. as applicant

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Related Devices (Code: FMF)

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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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