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FDA 510(k)

CHEMOTHERAPY WASTE DISPOSAL CONTAINERS

K-Number: K943658 · 1995-03-22

Decision Date1995-03-22
Product CodeMMK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CHEMOTHERAPY WASTE DISPOSAL CONTAINERS is the device name listed in this FDA 510(k) record. The listed applicant is Sage Products, Inc.. It received FDA 510(k) clearance on 1995-03-22 under 510(k) number K943658. 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 CHEMOTHERAPY WASTE DISPOSAL CONTAINERS?

CHEMOTHERAPY WASTE DISPOSAL CONTAINERS is a medical device that received FDA 510(k) clearance on 1995-03-22. The listed applicant is Sage Products, Inc.. The 510(k) number is K943658.

When did CHEMOTHERAPY WASTE DISPOSAL CONTAINERS receive FDA 510(k) clearance?

CHEMOTHERAPY WASTE DISPOSAL CONTAINERS received FDA 510(k) clearance on 1995-03-22, under 510(k) number K943658.

Who is the listed applicant for CHEMOTHERAPY WASTE DISPOSAL CONTAINERS?

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

What is the FDA product code for CHEMOTHERAPY WASTE DISPOSAL CONTAINERS?

The FDA product code for CHEMOTHERAPY WASTE DISPOSAL CONTAINERS 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 Sage Products, 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.

View all 31 devices →

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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