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FDA 510(k)

SIEMENS QUANTUM 7E11 TRANSRECTAL TRANSDUCER

K-Number: K930052 · 1995-01-04

ApplicantSiemens Quantum, Inc.
Decision Date1995-01-04
Product CodeITX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SIEMENS QUANTUM 7E11 TRANSRECTAL TRANSDUCER is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Quantum, Inc.. It received FDA 510(k) clearance on 1995-01-04 under 510(k) number K930052. The device is classified under product code ITX. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIEMENS QUANTUM 7E11 TRANSRECTAL TRANSDUCER?

SIEMENS QUANTUM 7E11 TRANSRECTAL TRANSDUCER is a medical device that received FDA 510(k) clearance on 1995-01-04. The listed applicant is Siemens Quantum, Inc.. The 510(k) number is K930052.

When did SIEMENS QUANTUM 7E11 TRANSRECTAL TRANSDUCER receive FDA 510(k) clearance?

SIEMENS QUANTUM 7E11 TRANSRECTAL TRANSDUCER received FDA 510(k) clearance on 1995-01-04, under 510(k) number K930052.

Who is the listed applicant for SIEMENS QUANTUM 7E11 TRANSRECTAL TRANSDUCER?

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

What is the FDA product code for SIEMENS QUANTUM 7E11 TRANSRECTAL TRANSDUCER?

The FDA product code for SIEMENS QUANTUM 7E11 TRANSRECTAL TRANSDUCER is ITX.

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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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