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FDA 510(k)

NEEDLE SYRINGE DISPOSAL DEVICE

K-Number: K896195 · 1989-11-27

ApplicantAdvanced Medical Components, Inc.
Decision Date1989-11-27
Product CodeMMK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

NEEDLE SYRINGE DISPOSAL DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Medical Components, Inc.. It received FDA 510(k) clearance on 1989-11-27 under 510(k) number K896195. The device is classified under product code MMK. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEEDLE SYRINGE DISPOSAL DEVICE?

NEEDLE SYRINGE DISPOSAL DEVICE is a medical device that received FDA 510(k) clearance on 1989-11-27. The listed applicant is Advanced Medical Components, Inc.. The 510(k) number is K896195.

When did NEEDLE SYRINGE DISPOSAL DEVICE receive FDA 510(k) clearance?

NEEDLE SYRINGE DISPOSAL DEVICE received FDA 510(k) clearance on 1989-11-27, under 510(k) number K896195.

Who is the listed applicant for NEEDLE SYRINGE DISPOSAL DEVICE?

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

What is the FDA product code for NEEDLE SYRINGE DISPOSAL DEVICE?

The FDA product code for NEEDLE SYRINGE DISPOSAL DEVICE is MMK.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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