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FDA 510(k)

VIDEO CAMERA W/ ELECTRONIC SHUTTER MODEL VCE-10

K-Number: K930053 · 1993-05-17

ApplicantMedical Devices, Inc.
Decision Date1993-05-17
Product CodeFWF
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

VIDEO CAMERA W/ ELECTRONIC SHUTTER MODEL VCE-10 is the device name listed in this FDA 510(k) record. The listed applicant is Medical Devices, Inc.. It received FDA 510(k) clearance on 1993-05-17 under 510(k) number K930053. 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 VIDEO CAMERA W/ ELECTRONIC SHUTTER MODEL VCE-10?

VIDEO CAMERA W/ ELECTRONIC SHUTTER MODEL VCE-10 is a medical device that received FDA 510(k) clearance on 1993-05-17. The listed applicant is Medical Devices, Inc.. The 510(k) number is K930053.

When did VIDEO CAMERA W/ ELECTRONIC SHUTTER MODEL VCE-10 receive FDA 510(k) clearance?

VIDEO CAMERA W/ ELECTRONIC SHUTTER MODEL VCE-10 received FDA 510(k) clearance on 1993-05-17, under 510(k) number K930053.

Who is the listed applicant for VIDEO CAMERA W/ ELECTRONIC SHUTTER MODEL VCE-10?

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

What is the FDA product code for VIDEO CAMERA W/ ELECTRONIC SHUTTER MODEL VCE-10?

The FDA product code for VIDEO CAMERA W/ ELECTRONIC SHUTTER MODEL VCE-10 is FWF.

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Other records listing Medical Devices, 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.

K002280PAD PRO PEDIATRIC ELECTRODE, MODEL PAD PRO 2602K930084MICRO-ARTHROSCOPEK940012SMARTBRACE ELECTRODEK943126ELECTROFLEXK935132HOME MICROCURRENT HMCK934619FLEXMATE

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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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