PATIENT EXAMINATION GLOVE— 510(k) K891956
Substantially EquivalentEquatorial Rubber Mfg. Industry Sdn Bhd
FDA 510(k) clearance K891956 for PATIENT EXAMINATION GLOVE, Substantially Equivalent on 1989-05-08. Applicant: Equatorial Rubber Mfg. Industry Sdn Bhd. Device class: 1.
Clearance details
- Applicant
- Equatorial Rubber Mfg. Industry Sdn Bhd
- 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
- Estate, 13600 P.W. Penang, MY
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Data sourced from openFDA. This site is unofficial and independent of the FDA.