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FDA 510(k)

STERISHARP 3-GALLON RSDC, MODEL RSDC3G

K-Number: K020664 · 2002-05-14

Decision Date2002-05-14
Product CodeMMK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

STERISHARP 3-GALLON RSDC, MODEL RSDC3G is the device name listed in this FDA 510(k) record. The listed applicant is Sterilogic Waste Systems, Inc.. It received FDA 510(k) clearance on 2002-05-14 under 510(k) number K020664. 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 STERISHARP 3-GALLON RSDC, MODEL RSDC3G?

STERISHARP 3-GALLON RSDC, MODEL RSDC3G is a medical device that received FDA 510(k) clearance on 2002-05-14. The listed applicant is Sterilogic Waste Systems, Inc.. The 510(k) number is K020664.

When did STERISHARP 3-GALLON RSDC, MODEL RSDC3G receive FDA 510(k) clearance?

STERISHARP 3-GALLON RSDC, MODEL RSDC3G received FDA 510(k) clearance on 2002-05-14, under 510(k) number K020664.

Who is the listed applicant for STERISHARP 3-GALLON RSDC, MODEL RSDC3G?

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

What is the FDA product code for STERISHARP 3-GALLON RSDC, MODEL RSDC3G?

The FDA product code for STERISHARP 3-GALLON RSDC, MODEL RSDC3G is MMK.

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.

Other records listing Sterilogic Waste Systems, Inc. as applicant

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: MMK)

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

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