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FDA 510(k)

MTH C/A MOBILE C ARM

K-Number: K827993 · 1982-09-13

ApplicantGeneral Medical Merate S.P.A
Decision Date1982-09-13
Product Code
DecisionSubstantially Equivalent

Device Summary

MTH C/A MOBILE C ARM is the device name listed in this FDA 510(k) record. The listed applicant is General Medical Merate S.P.A. It received FDA 510(k) clearance on 1982-09-13 under 510(k) number K827993. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MTH C/A MOBILE C ARM?

MTH C/A MOBILE C ARM is a medical device that received FDA 510(k) clearance on 1982-09-13. The listed applicant is General Medical Merate S.P.A. The 510(k) number is K827993.

When did MTH C/A MOBILE C ARM receive FDA 510(k) clearance?

MTH C/A MOBILE C ARM received FDA 510(k) clearance on 1982-09-13, under 510(k) number K827993.

Who is the listed applicant for MTH C/A MOBILE C ARM?

The FDA 510(k) record lists General Medical Merate S.P.A as the applicant. This does not by itself establish the device manufacturer.

Related Clinical Trials

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Other records listing General Medical Merate S.P.A 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.

K213081CLISIS SYSTEMS, Discovery RF180K173395MECALL CLISIS SYSTEMS, Discovery RF180K082243PRECISION RXI ANALOG AND DIGITAL X-RAY SYSTEMSK041605PRECISION RXI ANALOG X-RAY SYSTEMK881386X-RAY GENERATING SYSTEM TF 1000

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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