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FDA 510(k)

ROTATOR;MALE-MALE, MALE-FEMALE

K-Number: K932251 · 1993-08-05

ApplicantMerit Medical Systems, Inc.
Decision Date1993-08-05
Product CodeDTR
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ROTATOR;MALE-MALE, MALE-FEMALE is the device name listed in this FDA 510(k) record. The listed applicant is Merit Medical Systems, Inc.. It received FDA 510(k) clearance on 1993-08-05 under 510(k) number K932251. The device is classified under product code DTR. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ROTATOR;MALE-MALE, MALE-FEMALE?

ROTATOR;MALE-MALE, MALE-FEMALE is a medical device that received FDA 510(k) clearance on 1993-08-05. The listed applicant is Merit Medical Systems, Inc.. The 510(k) number is K932251.

When did ROTATOR;MALE-MALE, MALE-FEMALE receive FDA 510(k) clearance?

ROTATOR;MALE-MALE, MALE-FEMALE received FDA 510(k) clearance on 1993-08-05, under 510(k) number K932251.

Who is the listed applicant for ROTATOR;MALE-MALE, MALE-FEMALE?

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

What is the FDA product code for ROTATOR;MALE-MALE, MALE-FEMALE?

The FDA product code for ROTATOR;MALE-MALE, MALE-FEMALE is DTR.

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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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