MP-01X-I DISPOSABLE FILTER KIT
K-Number: K862790 · 1986-08-01
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Device Summary
Frequently Asked Questions
What is the MP-01X-I DISPOSABLE FILTER KIT?
MP-01X-I DISPOSABLE FILTER KIT is a medical device that received FDA 510(k) clearance on 1986-08-01. The listed applicant is Medipart Jerry Alexander. The 510(k) number is K862790.
When did MP-01X-I DISPOSABLE FILTER KIT receive FDA 510(k) clearance?
MP-01X-I DISPOSABLE FILTER KIT received FDA 510(k) clearance on 1986-08-01, under 510(k) number K862790.
Who is the listed applicant for MP-01X-I DISPOSABLE FILTER KIT?
The FDA 510(k) record lists Medipart Jerry Alexander as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MP-01X-I DISPOSABLE FILTER KIT?
The FDA product code for MP-01X-I DISPOSABLE FILTER KIT is CAH.
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 Medipart Jerry Alexander 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: CAH)
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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