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FDA 510(k)

ARTHROSCAN VIDEO SYSTEM

K-Number: K834069 · 1984-01-27

ApplicantConcept, Inc.
Decision Date1984-01-27
Product CodeFWF
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ARTHROSCAN VIDEO SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Concept, Inc.. It received FDA 510(k) clearance on 1984-01-27 under 510(k) number K834069. The device is classified under product code FWF. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARTHROSCAN VIDEO SYSTEM?

ARTHROSCAN VIDEO SYSTEM is a medical device that received FDA 510(k) clearance on 1984-01-27. The listed applicant is Concept, Inc.. The 510(k) number is K834069.

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

ARTHROSCAN VIDEO SYSTEM received FDA 510(k) clearance on 1984-01-27, under 510(k) number K834069.

Who is the listed applicant for ARTHROSCAN VIDEO SYSTEM?

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

What is the FDA product code for ARTHROSCAN VIDEO SYSTEM?

The FDA product code for ARTHROSCAN VIDEO SYSTEM is FWF.

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Other records listing Concept, 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.

K912640CONCEPT ENDOSTEAL FIXATION DEVICEK912957CONCEPT MICROMILLK896648CONCEPT UNICOMPARTMENTAL KNEE SYSTEMK894929STAPLE FIXATION SYSTEMK892376INTRAVISION(TM) ARTHROSCOPE SYSTEM (ADD'L APPLI.)K891109PANDA(R) NEEDLE CATHETER JEJUNOSTOMY TUBE

View all 83 devices →

Related Devices (Code: FWF)

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.

K053412FLEXISCOPE, MODELS 50MH AND 50 MHCSchoelly Imaging, Inc.K990154KARL STORZ DIRECT COUPLED INTERFACE (DCI 5) CAMERA SYSTEMKarl Storz Imaging, Inc.K982754EC-1000-7 DIGITAL ENDOSCOPY VIDEO CAMERA, MODELS EC 1000-7P (PAL) & EC 1000-7N (NTSC)A.Stein - Regulatory Affairs ConsultingK982965ENDOCAM CAMERA SYSTEMS 5502/5507 WITH CR CAMERA HEADS AND ACCESSORIESRichard Wolf Medical Instruments Corp.K982397VES 3001-M COMPLETE VIDEO ENDOSCOPIC SYSTEMAngiolaz, Inc.K982409VES 1501-MAngiolaz, 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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