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FDA 510(k)

LAST IMAGE HOLD

K-Number: K951942 · 1996-04-08

ApplicantInsight Systems
Decision Date1996-04-08
Product CodeLMB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

LAST IMAGE HOLD is the device name listed in this FDA 510(k) record. The listed applicant is Insight Systems. It received FDA 510(k) clearance on 1996-04-08 under 510(k) number K951942. The device is classified under product code LMB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LAST IMAGE HOLD?

LAST IMAGE HOLD is a medical device that received FDA 510(k) clearance on 1996-04-08. The listed applicant is Insight Systems. The 510(k) number is K951942.

When did LAST IMAGE HOLD receive FDA 510(k) clearance?

LAST IMAGE HOLD received FDA 510(k) clearance on 1996-04-08, under 510(k) number K951942.

Who is the listed applicant for LAST IMAGE HOLD?

The FDA 510(k) record lists Insight Systems as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LAST IMAGE HOLD?

The FDA product code for LAST IMAGE HOLD is LMB.

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Related Devices (Code: LMB)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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