PATIENT EXAMINATION GLOVE (LATEX)— 510(k) K891136
Substantially EquivalentAdvance Rubber, Inc.
FDA 510(k) clearance K891136 for PATIENT EXAMINATION GLOVE (LATEX), Substantially Equivalent on 1989-08-22. Applicant: Advance Rubber, Inc.. Device class: 1.
Clearance details
- Applicant
- Advance Rubber, 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
- Taipei, Taiwan R.O.C., TW
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More clearances from Advance Rubber, Inc.
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