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FDA 510(k)

DIGISCAN 2 PLUS

K-Number: K955457 · 1996-06-18

ApplicantSiemens Medical Solutions USA, Inc.
Decision Date1996-06-18
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DIGISCAN 2 PLUS 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 1996-06-18 under 510(k) number K955457. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIGISCAN 2 PLUS?

DIGISCAN 2 PLUS is a medical device that received FDA 510(k) clearance on 1996-06-18. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K955457.

When did DIGISCAN 2 PLUS receive FDA 510(k) clearance?

DIGISCAN 2 PLUS received FDA 510(k) clearance on 1996-06-18, under 510(k) number K955457.

Who is the listed applicant for DIGISCAN 2 PLUS?

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 DIGISCAN 2 PLUS?

The FDA product code for DIGISCAN 2 PLUS is LLZ.

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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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