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FDA 510(k)

ND VISION-220 ADAPTIVE IMAGE PROCESSESSOR

K-Number: K960301 · 1996-09-30

ApplicantDel Medical Systems Corp.
Decision Date1996-09-30
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ND VISION-220 ADAPTIVE IMAGE PROCESSESSOR is the device name listed in this FDA 510(k) record. The listed applicant is Del Medical Systems Corp.. It received FDA 510(k) clearance on 1996-09-30 under 510(k) number K960301. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ND VISION-220 ADAPTIVE IMAGE PROCESSESSOR?

ND VISION-220 ADAPTIVE IMAGE PROCESSESSOR is a medical device that received FDA 510(k) clearance on 1996-09-30. The listed applicant is Del Medical Systems Corp.. The 510(k) number is K960301.

When did ND VISION-220 ADAPTIVE IMAGE PROCESSESSOR receive FDA 510(k) clearance?

ND VISION-220 ADAPTIVE IMAGE PROCESSESSOR received FDA 510(k) clearance on 1996-09-30, under 510(k) number K960301.

Who is the listed applicant for ND VISION-220 ADAPTIVE IMAGE PROCESSESSOR?

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

What is the FDA product code for ND VISION-220 ADAPTIVE IMAGE PROCESSESSOR?

The FDA product code for ND VISION-220 ADAPTIVE IMAGE PROCESSESSOR is GCJ.

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Other records listing Del Medical Systems Corp. as applicant

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Related Devices (Code: GCJ)

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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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