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FDA 510(k)

SHARP-SAFE, BIODEGRADEABLE,DISP., NEEDLE DISP. BOX

K-Number: K901321 · 1990-05-11

ApplicantSharp Safe, Inc.
Decision Date1990-05-11
Product CodeLDQ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SHARP-SAFE, BIODEGRADEABLE,DISP., NEEDLE DISP. BOX is the device name listed in this FDA 510(k) record. The listed applicant is Sharp Safe, Inc.. It received FDA 510(k) clearance on 1990-05-11 under 510(k) number K901321. The device is classified under product code LDQ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SHARP-SAFE, BIODEGRADEABLE,DISP., NEEDLE DISP. BOX?

SHARP-SAFE, BIODEGRADEABLE,DISP., NEEDLE DISP. BOX is a medical device that received FDA 510(k) clearance on 1990-05-11. The listed applicant is Sharp Safe, Inc.. The 510(k) number is K901321.

When did SHARP-SAFE, BIODEGRADEABLE,DISP., NEEDLE DISP. BOX receive FDA 510(k) clearance?

SHARP-SAFE, BIODEGRADEABLE,DISP., NEEDLE DISP. BOX received FDA 510(k) clearance on 1990-05-11, under 510(k) number K901321.

Who is the listed applicant for SHARP-SAFE, BIODEGRADEABLE,DISP., NEEDLE DISP. BOX?

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

What is the FDA product code for SHARP-SAFE, BIODEGRADEABLE,DISP., NEEDLE DISP. BOX?

The FDA product code for SHARP-SAFE, BIODEGRADEABLE,DISP., NEEDLE DISP. BOX is LDQ.

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Related Devices (Code: LDQ)

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.

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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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