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FDA 510(k)

ISG MEDICAL IMAGING FAMILY OF WORKSTATIONS (MIFW)

K-Number: K941933 · 1994-07-29

ApplicantI.S.G. Technologies, Inc.
Decision Date1994-07-29
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ISG MEDICAL IMAGING FAMILY OF WORKSTATIONS (MIFW) is the device name listed in this FDA 510(k) record. The listed applicant is I.S.G. Technologies, Inc.. It received FDA 510(k) clearance on 1994-07-29 under 510(k) number K941933. 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 ISG MEDICAL IMAGING FAMILY OF WORKSTATIONS (MIFW)?

ISG MEDICAL IMAGING FAMILY OF WORKSTATIONS (MIFW) is a medical device that received FDA 510(k) clearance on 1994-07-29. The listed applicant is I.S.G. Technologies, Inc.. The 510(k) number is K941933.

When did ISG MEDICAL IMAGING FAMILY OF WORKSTATIONS (MIFW) receive FDA 510(k) clearance?

ISG MEDICAL IMAGING FAMILY OF WORKSTATIONS (MIFW) received FDA 510(k) clearance on 1994-07-29, under 510(k) number K941933.

Who is the listed applicant for ISG MEDICAL IMAGING FAMILY OF WORKSTATIONS (MIFW)?

The FDA 510(k) record lists I.S.G. Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ISG MEDICAL IMAGING FAMILY OF WORKSTATIONS (MIFW)?

The FDA product code for ISG MEDICAL IMAGING FAMILY OF WORKSTATIONS (MIFW) is LLZ.

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Other records listing I.S.G. Technologies, 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.

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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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