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FDA 510(k)

37-701-1 PATIENT DOASE MONITOR WITH DETECTORS

K-Number: K860469 · 1986-04-16

ApplicantVictoreen, Inc.
Decision Date1986-04-16
Product CodeKPZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

37-701-1 PATIENT DOASE MONITOR WITH DETECTORS is the device name listed in this FDA 510(k) record. The listed applicant is Victoreen, Inc.. It received FDA 510(k) clearance on 1986-04-16 under 510(k) number K860469. The device is classified under product code KPZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 37-701-1 PATIENT DOASE MONITOR WITH DETECTORS?

37-701-1 PATIENT DOASE MONITOR WITH DETECTORS is a medical device that received FDA 510(k) clearance on 1986-04-16. The listed applicant is Victoreen, Inc.. The 510(k) number is K860469.

When did 37-701-1 PATIENT DOASE MONITOR WITH DETECTORS receive FDA 510(k) clearance?

37-701-1 PATIENT DOASE MONITOR WITH DETECTORS received FDA 510(k) clearance on 1986-04-16, under 510(k) number K860469.

Who is the listed applicant for 37-701-1 PATIENT DOASE MONITOR WITH DETECTORS?

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 37-701-1 PATIENT DOASE MONITOR WITH DETECTORS?

The FDA product code for 37-701-1 PATIENT DOASE MONITOR WITH DETECTORS is KPZ.

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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 37-185K964952VERIDOSE V (FIVE), MODEL NUMBER 37-705K964785VERIDOSE DIODESK971382PRONE BREAST POSITIONING BOARD, MODEL #37-018

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Related Devices (Code: KPZ)

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.

K912249PATIENT DOSE MONITORTheta Systems, Inc.K854410VERIFLEXOld Delft Corp. of America

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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