PREPARE CARTRIDGE
K-Number: K023890 · 2003-02-07
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Device Summary
Frequently Asked Questions
What is the PREPARE CARTRIDGE?
PREPARE CARTRIDGE is a medical device that received FDA 510(k) clearance on 2003-02-07. The listed applicant is Appro Healthcare, Inc.. The 510(k) number is K023890.
When did PREPARE CARTRIDGE receive FDA 510(k) clearance?
PREPARE CARTRIDGE received FDA 510(k) clearance on 2003-02-07, under 510(k) number K023890.
Who is the listed applicant for PREPARE CARTRIDGE?
The FDA 510(k) record lists Appro Healthcare, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PREPARE CARTRIDGE?
The FDA product code for PREPARE CARTRIDGE is MRZ.
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 Appro Healthcare, 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: MRZ)
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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