FDA 510(k)

DIMENSIONALL ROTATOR

K-Number: K790753 · 1979-06-28

Decision Date1979-06-28

Product CodeJRQ

Advisory CommitteeCH

DecisionSubstantially Equivalent

Device Summary

DIMENSIONALL ROTATOR is the device name listed in this FDA 510(k) record. The listed applicant is American Hospital Supply Corp.. It received FDA 510(k) clearance on 1979-06-28 under 510(k) number K790753. The device is classified under product code JRQ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIMENSIONALL ROTATOR?

DIMENSIONALL ROTATOR is a medical device that received FDA 510(k) clearance on 1979-06-28. The listed applicant is American Hospital Supply Corp.. The 510(k) number is K790753.

When did DIMENSIONALL ROTATOR receive FDA 510(k) clearance?

DIMENSIONALL ROTATOR received FDA 510(k) clearance on 1979-06-28, under 510(k) number K790753.

Who is the listed applicant for DIMENSIONALL ROTATOR?

The FDA 510(k) record lists American Hospital Supply Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DIMENSIONALL ROTATOR?

The FDA product code for DIMENSIONALL ROTATOR is JRQ.

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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.