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FDA 510(k)

SIEMENS INTRAVAGINAL TRANSDUCER

K-Number: K885061 · 1989-02-23

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date1989-02-23
Product CodeHEM
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

SIEMENS INTRAVAGINAL TRANSDUCER is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 1989-02-23 under 510(k) number K885061. The device is classified under product code HEM. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIEMENS INTRAVAGINAL TRANSDUCER?

SIEMENS INTRAVAGINAL TRANSDUCER is a medical device that received FDA 510(k) clearance on 1989-02-23. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K885061.

When did SIEMENS INTRAVAGINAL TRANSDUCER receive FDA 510(k) clearance?

SIEMENS INTRAVAGINAL TRANSDUCER received FDA 510(k) clearance on 1989-02-23, under 510(k) number K885061.

Who is the listed applicant for SIEMENS INTRAVAGINAL TRANSDUCER?

The FDA 510(k) record lists Siemens Medical Solutions USA, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SIEMENS INTRAVAGINAL TRANSDUCER?

The FDA product code for SIEMENS INTRAVAGINAL TRANSDUCER is HEM.

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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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