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FDA 510(k)

CP FLEXIBLE COILS/ LP CIRCULAR FLEX COILS

K-Number: K935752 · 1994-03-29

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date1994-03-29
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CP FLEXIBLE COILS/ LP CIRCULAR FLEX COILS 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 1994-03-29 under 510(k) number K935752. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CP FLEXIBLE COILS/ LP CIRCULAR FLEX COILS?

CP FLEXIBLE COILS/ LP CIRCULAR FLEX COILS is a medical device that received FDA 510(k) clearance on 1994-03-29. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K935752.

When did CP FLEXIBLE COILS/ LP CIRCULAR FLEX COILS receive FDA 510(k) clearance?

CP FLEXIBLE COILS/ LP CIRCULAR FLEX COILS received FDA 510(k) clearance on 1994-03-29, under 510(k) number K935752.

Who is the listed applicant for CP FLEXIBLE COILS/ LP CIRCULAR FLEX COILS?

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 CP FLEXIBLE COILS/ LP CIRCULAR FLEX COILS?

The FDA product code for CP FLEXIBLE COILS/ LP CIRCULAR FLEX COILS is LNH.

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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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