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FDA 510(k)

SIENET ARCHIVE SERVER, ISA I, ISA II STORAGE SERVE

K-Number: K920310 · 1992-03-30

ApplicantSiemens Gammasonics, Inc.
Decision Date1992-03-30
Product CodeLMD
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SIENET ARCHIVE SERVER, ISA I, ISA II STORAGE SERVE is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Gammasonics, Inc.. It received FDA 510(k) clearance on 1992-03-30 under 510(k) number K920310. The device is classified under product code LMD. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIENET ARCHIVE SERVER, ISA I, ISA II STORAGE SERVE?

SIENET ARCHIVE SERVER, ISA I, ISA II STORAGE SERVE is a medical device that received FDA 510(k) clearance on 1992-03-30. The listed applicant is Siemens Gammasonics, Inc.. The 510(k) number is K920310.

When did SIENET ARCHIVE SERVER, ISA I, ISA II STORAGE SERVE receive FDA 510(k) clearance?

SIENET ARCHIVE SERVER, ISA I, ISA II STORAGE SERVE received FDA 510(k) clearance on 1992-03-30, under 510(k) number K920310.

Who is the listed applicant for SIENET ARCHIVE SERVER, ISA I, ISA II STORAGE SERVE?

The FDA 510(k) record lists Siemens Gammasonics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SIENET ARCHIVE SERVER, ISA I, ISA II STORAGE SERVE?

The FDA product code for SIENET ARCHIVE SERVER, ISA I, ISA II STORAGE SERVE is LMD.

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Other records listing Siemens Gammasonics, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K934766CARBON FIBER PALLETK933664POLYTRON T.O.P. (TIME, OPERATION, PERFORMANCE)K933256FAN BEAM COLLIMATORK920319SIENET IMAGE DISPLAY WORKSTATIONS, IMAGE ACQUISITIK923582SIENET CAMERA SERVERK922373MULTISPECT(TM) 2 DUAL DETECTOR CAMERA SYSTEM

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Related Devices (Code: LMD)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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