PATIENT EXAMINATION GLOVES— 510(k) K891313
Substantially EquivalentDr. Boo Co., Ltd.
FDA 510(k) clearance K891313 for PATIENT EXAMINATION GLOVES, Substantially Equivalent on 1989-05-04. Applicant: Dr. Boo Co., Ltd.. Device class: 1.
Clearance details
- Applicant
- Dr. Boo Co., 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
- Bangkok 10500, Thailand, TH
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More clearances from Dr. Boo Co., Ltd.
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