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FDA 510(k)

SYRINGE DISPOSAL SYSTEM

K-Number: K900687 · 1990-05-18

Decision Date1990-05-18
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SYRINGE DISPOSAL SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is National Syringe Disposal, Inc.. It received FDA 510(k) clearance on 1990-05-18 under 510(k) number K900687. 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 DISPOSAL SYSTEM?

SYRINGE DISPOSAL SYSTEM is a medical device that received FDA 510(k) clearance on 1990-05-18. The listed applicant is National Syringe Disposal, Inc.. The 510(k) number is K900687.

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

SYRINGE DISPOSAL SYSTEM received FDA 510(k) clearance on 1990-05-18, under 510(k) number K900687.

Who is the listed applicant for SYRINGE DISPOSAL SYSTEM?

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

What is the FDA product code for SYRINGE DISPOSAL SYSTEM?

The FDA product code for SYRINGE DISPOSAL SYSTEM is FMF.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: FMF)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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