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FDA 510(k)

MINGO LOG 7

K-Number: K843440 · 1984-09-04

ApplicantSiemens Elema AB
Decision Date1984-09-04
Product CodeDJH
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

MINGO LOG 7 is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Elema AB. It received FDA 510(k) clearance on 1984-09-04 under 510(k) number K843440. The device is classified under product code DJH. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MINGO LOG 7?

MINGO LOG 7 is a medical device that received FDA 510(k) clearance on 1984-09-04. The listed applicant is Siemens Elema AB. The 510(k) number is K843440.

When did MINGO LOG 7 receive FDA 510(k) clearance?

MINGO LOG 7 received FDA 510(k) clearance on 1984-09-04, under 510(k) number K843440.

Who is the listed applicant for MINGO LOG 7?

The FDA 510(k) record lists Siemens Elema AB as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MINGO LOG 7?

The FDA product code for MINGO LOG 7 is DJH.

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Other records listing Siemens Elema AB 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.

K023354COMPRESSOR MINI, 115 V, MODEL 64 81 779 EH81EK010923KION ANAESTHESIA SYSTEM, MODEL 65 03 879 E392EK010925SERVOI VENTILATOR SYSTEM, MODEL 64 87 800 E407EK002137CATHCOR DESKTOPK001315MODIFICATION TO KION ANESTHESIA SYSTEMK970839SERVO VENTILATOR 300A

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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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