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FDA 510(k)

POWER PACK 350/BATTERY PACK 351

K-Number: K923992 · 1993-04-13

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date1993-04-13
Product CodeCBK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

POWER PACK 350/BATTERY PACK 351 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 1993-04-13 under 510(k) number K923992. The device is classified under product code CBK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POWER PACK 350/BATTERY PACK 351?

POWER PACK 350/BATTERY PACK 351 is a medical device that received FDA 510(k) clearance on 1993-04-13. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K923992.

When did POWER PACK 350/BATTERY PACK 351 receive FDA 510(k) clearance?

POWER PACK 350/BATTERY PACK 351 received FDA 510(k) clearance on 1993-04-13, under 510(k) number K923992.

Who is the listed applicant for POWER PACK 350/BATTERY PACK 351?

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 POWER PACK 350/BATTERY PACK 351?

The FDA product code for POWER PACK 350/BATTERY PACK 351 is CBK.

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Related Devices (Code: CBK)

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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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