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FDA 510(k)

LASER BEAM LOCALIZER FOR SIREMOBIL 4

K-Number: K912380 · 1991-07-19

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date1991-07-19
Product CodeJAA
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

LASER BEAM LOCALIZER FOR SIREMOBIL 4 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 1991-07-19 under 510(k) number K912380. 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 LASER BEAM LOCALIZER FOR SIREMOBIL 4?

LASER BEAM LOCALIZER FOR SIREMOBIL 4 is a medical device that received FDA 510(k) clearance on 1991-07-19. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K912380.

When did LASER BEAM LOCALIZER FOR SIREMOBIL 4 receive FDA 510(k) clearance?

LASER BEAM LOCALIZER FOR SIREMOBIL 4 received FDA 510(k) clearance on 1991-07-19, under 510(k) number K912380.

Who is the listed applicant for LASER BEAM LOCALIZER FOR SIREMOBIL 4?

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 LASER BEAM LOCALIZER FOR SIREMOBIL 4?

The FDA product code for LASER BEAM LOCALIZER FOR SIREMOBIL 4 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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