PATIENT EXAMINATION GLOVE (LATEX)— 510(k) K891433
Substantially EquivalentJustin Intl., Inc.
FDA 510(k) clearance K891433 for PATIENT EXAMINATION GLOVE (LATEX), Substantially Equivalent on 1989-04-27. Applicant: Justin Intl., Inc.. Device class: 1.
Clearance details
- Applicant
- Justin Intl., Inc.
- 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
- New York, NY, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.