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FDA 510(k)

MINITROP AEROSAL, PRODOMO AEROSAL AND

K-Number: K830913 · 1983-05-25

ApplicantMedlog GmbH Marketing Services
Decision Date1983-05-25
Product CodeBTT
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MINITROP AEROSAL, PRODOMO AEROSAL AND is the device name listed in this FDA 510(k) record. The listed applicant is Medlog GmbH Marketing Services. It received FDA 510(k) clearance on 1983-05-25 under 510(k) number K830913. The device is classified under product code BTT. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MINITROP AEROSAL, PRODOMO AEROSAL AND?

MINITROP AEROSAL, PRODOMO AEROSAL AND is a medical device that received FDA 510(k) clearance on 1983-05-25. The listed applicant is Medlog GmbH Marketing Services. The 510(k) number is K830913.

When did MINITROP AEROSAL, PRODOMO AEROSAL AND receive FDA 510(k) clearance?

MINITROP AEROSAL, PRODOMO AEROSAL AND received FDA 510(k) clearance on 1983-05-25, under 510(k) number K830913.

Who is the listed applicant for MINITROP AEROSAL, PRODOMO AEROSAL AND?

The FDA 510(k) record lists Medlog GmbH Marketing Services as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MINITROP AEROSAL, PRODOMO AEROSAL AND?

The FDA product code for MINITROP AEROSAL, PRODOMO AEROSAL AND is BTT.

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Other records listing Medlog GmbH Marketing Services 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.

K832086USE 77 ULTRASONIC NEBULIZERK831325NUTROMATK813455PUMP & DETECTORK810155DOP 84

Related Devices (Code: BTT)

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.

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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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