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FDA 510(k)

DIASCOPE 2

K-Number: K833689 · 1984-10-26

ApplicantS & W Medico Teknik
Decision Date1984-10-26
Product CodeDRT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DIASCOPE 2 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 1984-10-26 under 510(k) number K833689. 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 DIASCOPE 2?

DIASCOPE 2 is a medical device that received FDA 510(k) clearance on 1984-10-26. The listed applicant is S & W Medico Teknik. The 510(k) number is K833689.

When did DIASCOPE 2 receive FDA 510(k) clearance?

DIASCOPE 2 received FDA 510(k) clearance on 1984-10-26, under 510(k) number K833689.

Who is the listed applicant for DIASCOPE 2?

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 DIASCOPE 2?

The FDA product code for DIASCOPE 2 is DRT.

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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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