MEDIPART DISPOS. MOUTHPIECE W/2MM I.D. MP-4410
K-Number: K853572 · 1985-10-29
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Device Summary
Frequently Asked Questions
What is the MEDIPART DISPOS. MOUTHPIECE W/2MM I.D. MP-4410?
MEDIPART DISPOS. MOUTHPIECE W/2MM I.D. MP-4410 is a medical device that received FDA 510(k) clearance on 1985-10-29. The listed applicant is Medipart Jerry Alexander. The 510(k) number is K853572.
When did MEDIPART DISPOS. MOUTHPIECE W/2MM I.D. MP-4410 receive FDA 510(k) clearance?
MEDIPART DISPOS. MOUTHPIECE W/2MM I.D. MP-4410 received FDA 510(k) clearance on 1985-10-29, under 510(k) number K853572.
Who is the listed applicant for MEDIPART DISPOS. MOUTHPIECE W/2MM I.D. MP-4410?
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 DISPOS. MOUTHPIECE W/2MM I.D. MP-4410?
The FDA product code for MEDIPART DISPOS. MOUTHPIECE W/2MM I.D. MP-4410 is BYP.
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: BYP)
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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