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FDA 510(k)

DOP 84

K-Number: K810155 · 1981-05-01

ApplicantMedlog GmbH Marketing Services
Decision Date1981-05-01
Product Code
DecisionSubstantially Equivalent

Device Summary

DOP 84 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 1981-05-01 under 510(k) number K810155. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DOP 84?

DOP 84 is a medical device that received FDA 510(k) clearance on 1981-05-01. The listed applicant is Medlog GmbH Marketing Services. The 510(k) number is K810155.

When did DOP 84 receive FDA 510(k) clearance?

DOP 84 received FDA 510(k) clearance on 1981-05-01, under 510(k) number K810155.

Who is the listed applicant for DOP 84?

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

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 NEBULIZERK831325NUTROMATK830913MINITROP AEROSAL, PRODOMO AEROSAL ANDK813455PUMP & DETECTOR

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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