SEAMLESS LATEX PATIENT EXAM GLOVES— 510(k) K920700
Substantially EquivalentDigitcare Corp.
FDA 510(k) clearance K920700 for SEAMLESS LATEX PATIENT EXAM GLOVES, Substantially Equivalent on 1992-05-11. Applicant: Digitcare Corp.. Device class: 1.
Clearance details
- Applicant
- Digitcare Corp.
- 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
- Beverly Hils, CA, US
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More clearances from Digitcare Corp.
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