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FDA 510(k)

MEDIPART MOUTHPIECE MP-1010

K-Number: K853575 · 1985-10-29

Decision Date1985-10-29
Product CodeBYP
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MEDIPART MOUTHPIECE MP-1010 is the device name listed in this FDA 510(k) record. The listed applicant is Medipart Jerry Alexander. It received FDA 510(k) clearance on 1985-10-29 under 510(k) number K853575. The device is classified under product code BYP. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDIPART MOUTHPIECE MP-1010?

MEDIPART MOUTHPIECE MP-1010 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 K853575.

When did MEDIPART MOUTHPIECE MP-1010 receive FDA 510(k) clearance?

MEDIPART MOUTHPIECE MP-1010 received FDA 510(k) clearance on 1985-10-29, under 510(k) number K853575.

Who is the listed applicant for MEDIPART MOUTHPIECE MP-1010?

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 MOUTHPIECE MP-1010?

The FDA product code for MEDIPART MOUTHPIECE MP-1010 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.

View all 49 devices →

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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