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FDA 510(k)

SIRESKOP CX

K-Number: K932445 · 1993-09-07

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date1993-09-07
Product CodeJAA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SIRESKOP CX 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 1993-09-07 under 510(k) number K932445. The device is classified under product code JAA. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIRESKOP CX?

SIRESKOP CX is a medical device that received FDA 510(k) clearance on 1993-09-07. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K932445.

When did SIRESKOP CX receive FDA 510(k) clearance?

SIRESKOP CX received FDA 510(k) clearance on 1993-09-07, under 510(k) number K932445.

Who is the listed applicant for SIRESKOP CX?

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 SIRESKOP CX?

The FDA product code for SIRESKOP CX is JAA.

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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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