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FDA 510(k)

MEDIPART RADIOAEROSOL DELIVERY SYS FOR ULTRAVENT S

K-Number: K854551 · 1985-12-19

Decision Date1985-12-19
Product CodeCCQ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MEDIPART RADIOAEROSOL DELIVERY SYS FOR ULTRAVENT S 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 1985-12-19 under 510(k) number K854551. The device is classified under product code CCQ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDIPART RADIOAEROSOL DELIVERY SYS FOR ULTRAVENT S?

MEDIPART RADIOAEROSOL DELIVERY SYS FOR ULTRAVENT S is a medical device that received FDA 510(k) clearance on 1985-12-19. The listed applicant is Medipart Jerry Alexander. The 510(k) number is K854551.

When did MEDIPART RADIOAEROSOL DELIVERY SYS FOR ULTRAVENT S receive FDA 510(k) clearance?

MEDIPART RADIOAEROSOL DELIVERY SYS FOR ULTRAVENT S received FDA 510(k) clearance on 1985-12-19, under 510(k) number K854551.

Who is the listed applicant for MEDIPART RADIOAEROSOL DELIVERY SYS FOR ULTRAVENT S?

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 RADIOAEROSOL DELIVERY SYS FOR ULTRAVENT S?

The FDA product code for MEDIPART RADIOAEROSOL DELIVERY SYS FOR ULTRAVENT S is CCQ.

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: CCQ)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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