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FDA 510(k)

SIEMENS ENDO-P-PROBE

K-Number: K894806 · 1989-10-05

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date1989-10-05
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SIEMENS ENDO-P-PROBE 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 1989-10-05 under 510(k) number K894806. 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 SIEMENS ENDO-P-PROBE?

SIEMENS ENDO-P-PROBE is a medical device that received FDA 510(k) clearance on 1989-10-05. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K894806.

When did SIEMENS ENDO-P-PROBE receive FDA 510(k) clearance?

SIEMENS ENDO-P-PROBE received FDA 510(k) clearance on 1989-10-05, under 510(k) number K894806.

Who is the listed applicant for SIEMENS ENDO-P-PROBE?

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 ENDO-P-PROBE?

The FDA product code for SIEMENS ENDO-P-PROBE is IYO.

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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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