ZOLL M SERIES ETCO2 OPTION
K-Number: K993036 · 2000-02-28
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Device Summary
Frequently Asked Questions
What is the ZOLL M SERIES ETCO2 OPTION?
ZOLL M SERIES ETCO2 OPTION is a medical device that received FDA 510(k) clearance on 2000-02-28. The listed applicant is Zoll Medical Corp. The 510(k) number is K993036.
When did ZOLL M SERIES ETCO2 OPTION receive FDA 510(k) clearance?
ZOLL M SERIES ETCO2 OPTION received FDA 510(k) clearance on 2000-02-28, under 510(k) number K993036.
Who is the listed applicant for ZOLL M SERIES ETCO2 OPTION?
The FDA 510(k) record lists Zoll Medical Corp as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ZOLL M SERIES ETCO2 OPTION?
The FDA product code for ZOLL M SERIES ETCO2 OPTION is MKJ. This falls under the Dental category.
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 Zoll Medical Corp 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: MKJ)
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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