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FDA 510(k)

POSI-TOT

K-Number: K790685 · 1979-04-23

ApplicantVictoreen, Inc.
Decision Date1979-04-23
Product CodeKPR
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

POSI-TOT is the device name listed in this FDA 510(k) record. The listed applicant is Victoreen, Inc.. It received FDA 510(k) clearance on 1979-04-23 under 510(k) number K790685. 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 POSI-TOT?

POSI-TOT is a medical device that received FDA 510(k) clearance on 1979-04-23. The listed applicant is Victoreen, Inc.. The 510(k) number is K790685.

When did POSI-TOT receive FDA 510(k) clearance?

POSI-TOT received FDA 510(k) clearance on 1979-04-23, under 510(k) number K790685.

Who is the listed applicant for POSI-TOT?

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 POSI-TOT?

The FDA product code for POSI-TOT is KPR.

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.

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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.

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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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