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FDA 510(k)

RESUBMITTED RADIOAEROSOL CONT. SYSTEM MP-963

K-Number: K893532 · 1989-08-21

Decision Date1989-08-21
Product CodeCBN
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

RESUBMITTED RADIOAEROSOL CONT. SYSTEM MP-963 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 1989-08-21 under 510(k) number K893532. The device is classified under product code CBN. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RESUBMITTED RADIOAEROSOL CONT. SYSTEM MP-963?

RESUBMITTED RADIOAEROSOL CONT. SYSTEM MP-963 is a medical device that received FDA 510(k) clearance on 1989-08-21. The listed applicant is Medipart Jerry Alexander. The 510(k) number is K893532.

When did RESUBMITTED RADIOAEROSOL CONT. SYSTEM MP-963 receive FDA 510(k) clearance?

RESUBMITTED RADIOAEROSOL CONT. SYSTEM MP-963 received FDA 510(k) clearance on 1989-08-21, under 510(k) number K893532.

Who is the listed applicant for RESUBMITTED RADIOAEROSOL CONT. SYSTEM MP-963?

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 RESUBMITTED RADIOAEROSOL CONT. SYSTEM MP-963?

The FDA product code for RESUBMITTED RADIOAEROSOL CONT. SYSTEM MP-963 is CBN.

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: CBN)

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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