LATEX EXAMINATION GLOVE— 510(k) K904324
Substantially EquivalentGallimore Ent., Inc.
FDA 510(k) clearance K904324 for LATEX EXAMINATION GLOVE, Substantially Equivalent on 1990-10-03. Applicant: Gallimore Ent., Inc.. Device class: 1.
Clearance details
- Applicant
- Gallimore Ent., 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
- Toronto Ont M3a 1b2, CA
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Data sourced from openFDA. This site is unofficial and independent of the FDA.