PATIENT EXAMINATION GLOVE (LATEX)— 510(k) K892035
Substantially EquivalentFine Spring Ent. Co., Ltd.
FDA 510(k) clearance K892035 for PATIENT EXAMINATION GLOVE (LATEX), Substantially Equivalent on 1989-09-12. Applicant: Fine Spring Ent. Co., Ltd.. Device class: 1.
Clearance details
- Applicant
- Fine Spring Ent. 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
- Seattle, WA, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.