ZOLL PROPAQ MD
K-Number: K102468 · 2010-09-30
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Device Summary
Frequently Asked Questions
What is the ZOLL PROPAQ MD?
ZOLL PROPAQ MD is a medical device that received FDA 510(k) clearance on 2010-09-30. The listed applicant is Zoll Medical Corporation, World Wide Headquarters. The 510(k) number is K102468.
When did ZOLL PROPAQ MD receive FDA 510(k) clearance?
ZOLL PROPAQ MD received FDA 510(k) clearance on 2010-09-30, under 510(k) number K102468.
Who is the listed applicant for ZOLL PROPAQ MD?
The FDA 510(k) record lists Zoll Medical Corporation, World Wide Headquarters as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ZOLL PROPAQ MD?
The FDA product code for ZOLL PROPAQ MD is LDD.
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 Corporation, World Wide Headquarters 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: LDD)
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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