MEDIPART FILTER & TUBING MP-02X
K-Number: K844491 · 1984-12-04
Advertisement
Device Summary
Frequently Asked Questions
What is the MEDIPART FILTER & TUBING MP-02X?
MEDIPART FILTER & TUBING MP-02X is a medical device that received FDA 510(k) clearance on 1984-12-04. The listed applicant is Medipart Jerry Alexander. The 510(k) number is K844491.
When did MEDIPART FILTER & TUBING MP-02X receive FDA 510(k) clearance?
MEDIPART FILTER & TUBING MP-02X received FDA 510(k) clearance on 1984-12-04, under 510(k) number K844491.
Who is the listed applicant for MEDIPART FILTER & TUBING MP-02X?
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 MEDIPART FILTER & TUBING MP-02X?
The FDA product code for MEDIPART FILTER & TUBING MP-02X 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.
Advertisement