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FDA 510(k)

MEDSTATION

K-Number: K973090 · 1997-10-28

ApplicantProgram S.R.L.
Decision Date1997-10-28
Product CodeLMD
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MEDSTATION is the device name listed in this FDA 510(k) record. The listed applicant is Program S.R.L.. It received FDA 510(k) clearance on 1997-10-28 under 510(k) number K973090. The device is classified under product code LMD. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDSTATION?

MEDSTATION is a medical device that received FDA 510(k) clearance on 1997-10-28. The listed applicant is Program S.R.L.. The 510(k) number is K973090.

When did MEDSTATION receive FDA 510(k) clearance?

MEDSTATION received FDA 510(k) clearance on 1997-10-28, under 510(k) number K973090.

Who is the listed applicant for MEDSTATION?

The FDA 510(k) record lists Program S.R.L. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEDSTATION?

The FDA product code for MEDSTATION is LMD.

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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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