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FDA 510(k)

TYPE 9140/NEO

K-Number: K896700 · 1990-04-20

ApplicantS & W Medico Teknik
Decision Date1990-04-20
Product CodeDRT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TYPE 9140/NEO is the device name listed in this FDA 510(k) record. The listed applicant is S & W Medico Teknik. It received FDA 510(k) clearance on 1990-04-20 under 510(k) number K896700. The device is classified under product code DRT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TYPE 9140/NEO?

TYPE 9140/NEO is a medical device that received FDA 510(k) clearance on 1990-04-20. The listed applicant is S & W Medico Teknik. The 510(k) number is K896700.

When did TYPE 9140/NEO receive FDA 510(k) clearance?

TYPE 9140/NEO received FDA 510(k) clearance on 1990-04-20, under 510(k) number K896700.

Who is the listed applicant for TYPE 9140/NEO?

The FDA 510(k) record lists S & W Medico Teknik as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TYPE 9140/NEO?

The FDA product code for TYPE 9140/NEO is DRT.

Other records listing S & W Medico Teknik as applicant

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Related Devices (Code: DRT)

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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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