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FDA 510(k)

MINGOCARD 7 & MINGOPHONE 7

K-Number: K822983 · 1982-11-24

ApplicantSiemens Corp.
Decision Date1982-11-24
Product CodeDSF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MINGOCARD 7 & MINGOPHONE 7 is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Corp.. It received FDA 510(k) clearance on 1982-11-24 under 510(k) number K822983. The device is classified under product code DSF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MINGOCARD 7 & MINGOPHONE 7?

MINGOCARD 7 & MINGOPHONE 7 is a medical device that received FDA 510(k) clearance on 1982-11-24. The listed applicant is Siemens Corp.. The 510(k) number is K822983.

When did MINGOCARD 7 & MINGOPHONE 7 receive FDA 510(k) clearance?

MINGOCARD 7 & MINGOPHONE 7 received FDA 510(k) clearance on 1982-11-24, under 510(k) number K822983.

Who is the listed applicant for MINGOCARD 7 & MINGOPHONE 7?

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

What is the FDA product code for MINGOCARD 7 & MINGOPHONE 7?

The FDA product code for MINGOCARD 7 & MINGOPHONE 7 is DSF.

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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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