LATEX PATIENT EXAMINATION GLOVE— 510(k) K895497
Substantially EquivalentPlymouth , Ltd.
FDA 510(k) clearance K895497 for LATEX PATIENT EXAMINATION GLOVE, Substantially Equivalent on 1989-11-21. Applicant: Plymouth , Ltd.. Device class: 1.
Clearance details
- Applicant
- Plymouth , Ltd.
- Product code
- Code LYY
- Device class
- Class 1
- Regulation
- 21 CFR 880.6250
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Wanchai, Hong Kong, HK
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Data sourced from openFDA. This site is unofficial and independent of the FDA.