LAS-R HUMAN IGE TEST— 510(k) K780753
Substantially EquivalentHyland Therapeutic Div., Travenol Laboratories
FDA 510(k) clearance K780753 for LAS-R HUMAN IGE TEST, Substantially Equivalent on 1978-06-06. Applicant: Hyland Therapeutic Div., Travenol Laboratories. Device class: 2.
Clearance details
- Applicant
- Hyland Therapeutic Div., Travenol Laboratories
- Product code
- Code DGC
- Device class
- Class 2
- Regulation
- 21 CFR 866.5510
- Advisory panel
- Immunology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
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