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FDA 510(k)

VERIDOSE V (FIVE), MODEL NUMBER 37-705

K-Number: K964952 · 1997-07-21

ApplicantVictoreen, Inc.
Decision Date1997-07-21
Product CodeJAD
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VERIDOSE V (FIVE), MODEL NUMBER 37-705 is the device name listed in this FDA 510(k) record. The listed applicant is Victoreen, Inc.. It received FDA 510(k) clearance on 1997-07-21 under 510(k) number K964952. The device is classified under product code JAD. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VERIDOSE V (FIVE), MODEL NUMBER 37-705?

VERIDOSE V (FIVE), MODEL NUMBER 37-705 is a medical device that received FDA 510(k) clearance on 1997-07-21. The listed applicant is Victoreen, Inc.. The 510(k) number is K964952.

When did VERIDOSE V (FIVE), MODEL NUMBER 37-705 receive FDA 510(k) clearance?

VERIDOSE V (FIVE), MODEL NUMBER 37-705 received FDA 510(k) clearance on 1997-07-21, under 510(k) number K964952.

Who is the listed applicant for VERIDOSE V (FIVE), MODEL NUMBER 37-705?

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

What is the FDA product code for VERIDOSE V (FIVE), MODEL NUMBER 37-705?

The FDA product code for VERIDOSE V (FIVE), MODEL NUMBER 37-705 is JAD.

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Other records listing Victoreen, 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.

K982937MODEL 580-006 RADIATION THERAPY IONIZATION CHAMBERK974112VACUDAP, MODEL 2000, 2001K973960MODEL 37-185K964785VERIDOSE DIODESK971382PRONE BREAST POSITIONING BOARD, MODEL #37-018K952233CLEAR-PB LEAD PLASTIC OVERHEAD BARRIER 56-628

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Related Devices (Code: JAD)

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.

K250692GentleBeam (GB1000)Voxel Ray Solutions, LLCK241174INTRABEAM (700); And accessories (INTRABEAM SMART Stand, INTRABEAM SMART Spherical Applicator, INTRABEAM Spherical Sizer Set, INTRABEAM Needle Applicator)Carl Zeiss Meditec, AGK230611X80 / RADiant / PhotoElectric Therapy System (RADiant Aura)Xstrahl, Ltd.K213942EsteyaNucletron B.V.K190255Sensus Healthcare TVM Balloon ApplicatorSensus Healthcare, Inc.K182641Sensus IORT SystemSensus Healthcare, 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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