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FDA 510(k)

DIAMENTOR PATIENT X-RAY EXPOSURE INDICATOR 07302

K-Number: K853753 · 1985-10-02

ApplicantVictoreen, Inc.
Decision Date1985-10-02
Product CodeKPR
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DIAMENTOR PATIENT X-RAY EXPOSURE INDICATOR 07302 is the device name listed in this FDA 510(k) record. The listed applicant is Victoreen, Inc.. It received FDA 510(k) clearance on 1985-10-02 under 510(k) number K853753. The device is classified under product code KPR. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIAMENTOR PATIENT X-RAY EXPOSURE INDICATOR 07302?

DIAMENTOR PATIENT X-RAY EXPOSURE INDICATOR 07302 is a medical device that received FDA 510(k) clearance on 1985-10-02. The listed applicant is Victoreen, Inc.. The 510(k) number is K853753.

When did DIAMENTOR PATIENT X-RAY EXPOSURE INDICATOR 07302 receive FDA 510(k) clearance?

DIAMENTOR PATIENT X-RAY EXPOSURE INDICATOR 07302 received FDA 510(k) clearance on 1985-10-02, under 510(k) number K853753.

Who is the listed applicant for DIAMENTOR PATIENT X-RAY EXPOSURE INDICATOR 07302?

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 DIAMENTOR PATIENT X-RAY EXPOSURE INDICATOR 07302?

The FDA product code for DIAMENTOR PATIENT X-RAY EXPOSURE INDICATOR 07302 is KPR.

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Other records listing Victoreen, Inc. as applicant

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Related Devices (Code: KPR)

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.

K260227EXSYS DEXi (EXSYS DEXi-S40S); EXSYS DEXi (EXSYS DEXi-S40P); EXSYS DEXi (EXSYS DEXi-S40T); EXSYS DEXi (EXSYS DEXi-S50HDRTECH CorporationK260488MULTIX Impact; MULTIX Impact CSiemens Medical Solutions USA, Inc.K260481GC85ASamsung Electronics Co., Ltd.K260482DRE DuoJpi Healthcare Co, Ltd.K253446AeroDR TX c02Dk Medical Systems Co., Ltd.K250954DRX-Evolution Plus X-ray System, DRX-Compass Mobile X-ray System, Lux HD 35 detector, Lux HD 43 detectorCarestream Health

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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