STERISHARP 2.5-GALLON RSDC, MODEL #RSDC2.5G
K-Number: K991612 · 1999-05-28
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Device Summary
Frequently Asked Questions
What is the STERISHARP 2.5-GALLON RSDC, MODEL #RSDC2.5G?
STERISHARP 2.5-GALLON RSDC, MODEL #RSDC2.5G is a medical device that received FDA 510(k) clearance on 1999-05-28. The listed applicant is Sterilogic Waste Systems, Inc.. The 510(k) number is K991612.
When did STERISHARP 2.5-GALLON RSDC, MODEL #RSDC2.5G receive FDA 510(k) clearance?
STERISHARP 2.5-GALLON RSDC, MODEL #RSDC2.5G received FDA 510(k) clearance on 1999-05-28, under 510(k) number K991612.
Who is the listed applicant for STERISHARP 2.5-GALLON RSDC, MODEL #RSDC2.5G?
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 2.5-GALLON RSDC, MODEL #RSDC2.5G?
The FDA product code for STERISHARP 2.5-GALLON RSDC, MODEL #RSDC2.5G 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
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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