PATIENT EXAMINATION GLOVE (LATEX)— 510(k) K892033
Substantially EquivalentWeiss Ent., Inc.
FDA 510(k) clearance K892033 for PATIENT EXAMINATION GLOVE (LATEX), Substantially Equivalent on 1989-08-10. Applicant: Weiss Ent., Inc..
Clearance details
- Applicant
- Weiss Ent., Inc.
- Product code
- Code LYY
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Santa Rosa, CA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.