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FDA 510(k)

SYRINGE W/NEEDLE COMBIN & SYRINGE ONLY

K-Number: K844106 · 1985-01-14

ApplicantAbco Dealers, Inc.
Decision Date1985-01-14
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SYRINGE W/NEEDLE COMBIN & SYRINGE ONLY 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 1985-01-14 under 510(k) number K844106. 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 SYRINGE W/NEEDLE COMBIN & SYRINGE ONLY?

SYRINGE W/NEEDLE COMBIN & SYRINGE ONLY is a medical device that received FDA 510(k) clearance on 1985-01-14. The listed applicant is Abco Dealers, Inc.. The 510(k) number is K844106.

When did SYRINGE W/NEEDLE COMBIN & SYRINGE ONLY receive FDA 510(k) clearance?

SYRINGE W/NEEDLE COMBIN & SYRINGE ONLY received FDA 510(k) clearance on 1985-01-14, under 510(k) number K844106.

Who is the listed applicant for SYRINGE W/NEEDLE COMBIN & SYRINGE ONLY?

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 SYRINGE W/NEEDLE COMBIN & SYRINGE ONLY?

The FDA product code for SYRINGE W/NEEDLE COMBIN & SYRINGE ONLY 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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