PATIENT EXAMINATION GLOVE— 510(k) K891017
Substantially EquivalentParamount Products, Inc.
FDA 510(k) clearance K891017 for PATIENT EXAMINATION GLOVE, Substantially Equivalent on 1989-04-06. Applicant: Paramount Products, Inc..
Clearance details
- Applicant
- Paramount Products, Inc.
- Product code
- Code LYY
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Miami, FL, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.