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FDA 510(k)

ENDOVAGINAL PROBE, SMS-510VA

K-Number: K882959 · 1988-08-18

ApplicantToshiba Medical Systems
Decision Date1988-08-18
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ENDOVAGINAL PROBE, SMS-510VA is the device name listed in this FDA 510(k) record. The listed applicant is Toshiba Medical Systems. It received FDA 510(k) clearance on 1988-08-18 under 510(k) number K882959. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENDOVAGINAL PROBE, SMS-510VA?

ENDOVAGINAL PROBE, SMS-510VA is a medical device that received FDA 510(k) clearance on 1988-08-18. The listed applicant is Toshiba Medical Systems. The 510(k) number is K882959.

When did ENDOVAGINAL PROBE, SMS-510VA receive FDA 510(k) clearance?

ENDOVAGINAL PROBE, SMS-510VA received FDA 510(k) clearance on 1988-08-18, under 510(k) number K882959.

Who is the listed applicant for ENDOVAGINAL PROBE, SMS-510VA?

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

What is the FDA product code for ENDOVAGINAL PROBE, SMS-510VA?

The FDA product code for ENDOVAGINAL PROBE, SMS-510VA is IYO.

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Other records listing Toshiba Medical Systems as applicant

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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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