PATIENT EXAMINATION GLOVES (LATEX)(POWDERED)
FDA 510(k) clearance K891640 · decided 1989-05-22
Clearance details
- K-number
- K891640
- Device name
- PATIENT EXAMINATION GLOVES (LATEX)(POWDERED)
- Applicant
- Perusahaan Getah Asas Sdn. Bhd.
- Decision
- Substantially Equivalent
- Date received
- 1989-03-17
- Decision date
- 1989-05-22
- Days to decision
- 66 days
- Clearance type
- Traditional
- Product code
- LYY
- Device class
- 1
- Regulation number
- 880.6250
- Medical specialty
- General Hospital
- Advisory committee
- General Hospital
- Location
- 42000 Port Kelang, S.D.E., MY
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.