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FDA 510(k)

VIDEO SYSTEM INTERFACE MODELS

K-Number: K904540 · 1990-10-26

ApplicantPerkins Mfg. Co.
Decision Date1990-10-26
Product CodeIZI
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VIDEO SYSTEM INTERFACE MODELS is the device name listed in this FDA 510(k) record. The listed applicant is Perkins Mfg. Co.. It received FDA 510(k) clearance on 1990-10-26 under 510(k) number K904540. The device is classified under product code IZI. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VIDEO SYSTEM INTERFACE MODELS?

VIDEO SYSTEM INTERFACE MODELS is a medical device that received FDA 510(k) clearance on 1990-10-26. The listed applicant is Perkins Mfg. Co.. The 510(k) number is K904540.

When did VIDEO SYSTEM INTERFACE MODELS receive FDA 510(k) clearance?

VIDEO SYSTEM INTERFACE MODELS received FDA 510(k) clearance on 1990-10-26, under 510(k) number K904540.

Who is the listed applicant for VIDEO SYSTEM INTERFACE MODELS?

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

What is the FDA product code for VIDEO SYSTEM INTERFACE MODELS?

The FDA product code for VIDEO SYSTEM INTERFACE MODELS is IZI.

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Other records listing Perkins Mfg. Co. 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.

K972136TV MONITOR (P12/17)K954222VIDEO ENHANCEMENT UNITK926348SC1000 SCAN CONVERTERK920550DISPLAY PROCESSOR - MODEL IDP5100K915232GRUNDIG ELECTRONICS VARIOUS MODELSK910384VIDEO ANNOTATOR MODEL PK2310

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Related Devices (Code: IZI)

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.

K261037780 nm SPY Portable Handheld Imaging (SPY-PHI) SystemStryker EndoscopyK253181SURGIMAGE SIM 1000H Fluorescence Imaging PlatformSurgimage CorporationK243645IC-Flow™ Imaging System 2.0Diagnostic Green GmbHK243077Affirm 800Digital Surgery Systems, Inc. (D.B.A True Digital Surgery)K231986Modus IRSynaptive Medical, Inc.K234090EXPLORER AIR® II (8001, 8002, 8003); EXPLORER AIR® Sterile Drape (8004)Surgvision GmbH

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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