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FDA 510(k)

S-41 & S-41S VIDEO IMAGING SYSTEM

K-Number: K962020 · 1996-08-30

ApplicantDel Medical Systems Corp.
Decision Date1996-08-30
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

S-41 & S-41S VIDEO IMAGING SYSTEM 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 1996-08-30 under 510(k) number K962020. 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 S-41 & S-41S VIDEO IMAGING SYSTEM?

S-41 & S-41S VIDEO IMAGING SYSTEM is a medical device that received FDA 510(k) clearance on 1996-08-30. The listed applicant is Del Medical Systems Corp.. The 510(k) number is K962020.

When did S-41 & S-41S VIDEO IMAGING SYSTEM receive FDA 510(k) clearance?

S-41 & S-41S VIDEO IMAGING SYSTEM received FDA 510(k) clearance on 1996-08-30, under 510(k) number K962020.

Who is the listed applicant for S-41 & S-41S VIDEO IMAGING SYSTEM?

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 S-41 & S-41S VIDEO IMAGING SYSTEM?

The FDA product code for S-41 & S-41S VIDEO IMAGING SYSTEM is GCJ.

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Other records listing Del Medical Systems Corp. 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.

K962684S-357 VIDEO IMAGING SYSTEMK960301ND VISION-220 ADAPTIVE IMAGE PROCESSESSORK962651S-52 ELECTRONIC VIDEO LAPAROSCOPEK962979S-53 INTRORAL DENTAL SYSTEMK962024S-57 VIDEO IMAGING SYSTEMK942924MSV-2000 VIDEO IMAGING SYSTEM

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Related Devices (Code: GCJ)

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.

K262397CuratOR EX2742Eizo CorporationK260884UNIDRIVE Select SystemKarl Storz SE & CO. KGK260972OEV-271MUH LCD Monitor;OEV-321MUH LCD Monitor;OEV-431MUH LCD MonitorSony CorporationK261139VereSee (VER150, VER200, VER151, VER201, VER200C, and VER-100-103)Freyja Healthcare, LLCK253541EZ-Close™ (EZ Close Port Site Closing Device, EZ Close MAX Port Site Closing Device, EZ Close II Port Site Closing Device)Medical ImpactK261614LED LCD Monitor (OEV-271H)Lg Electronics.Inc

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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