ROTATOR; MALE-MALE, MALE-FEMALE— 510(k) K932251
Substantially EquivalentMerit Medical Systems, Inc.
FDA 510(k) clearance K932251 for ROTATOR; MALE-MALE, MALE-FEMALE, Substantially Equivalent on 1993-08-05. Applicant: Merit Medical Systems, Inc.. Device class: 2.
Clearance details
- Device name as filed
- ROTATOR;MALE-MALE, MALE-FEMALE
- Applicant
- Merit Medical Systems, Inc.
- Product code
- Code DTR
- Device class
- Class 2
- Regulation
- 21 CFR 870.4240
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Salt Lake City, UT, US
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More clearances from Merit Medical Systems, Inc.
view allAdverse events under product code DTR
product code DTR- Other
- 1
- Total
- 1
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.