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FDA 510(k)

PACSNET RESEARCH TOOLKIT

K-Number: K905199 · 1991-01-14

Decision Date1991-01-14
Product CodeLMD
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PACSNET RESEARCH TOOLKIT 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 1991-01-14 under 510(k) number K905199. 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 PACSNET RESEARCH TOOLKIT?

PACSNET RESEARCH TOOLKIT is a medical device that received FDA 510(k) clearance on 1991-01-14. The listed applicant is Siemens Gammasonics, Inc.. The 510(k) number is K905199.

When did PACSNET RESEARCH TOOLKIT receive FDA 510(k) clearance?

PACSNET RESEARCH TOOLKIT received FDA 510(k) clearance on 1991-01-14, under 510(k) number K905199.

Who is the listed applicant for PACSNET RESEARCH TOOLKIT?

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 PACSNET RESEARCH TOOLKIT?

The FDA product code for PACSNET RESEARCH TOOLKIT is LMD.

Related Clinical Trials

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.

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.

View all 53 devices →

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.

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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