OCCULT-ALERT— 510(k) K830919
Substantially EquivalentBeta Med Pharmaceuticals, Inc.
FDA 510(k) clearance K830919 for OCCULT-ALERT, Substantially Equivalent on 1983-07-07. Applicant: Beta Med Pharmaceuticals, Inc.. Device class: 2.
Clearance details
- Applicant
- Beta Med Pharmaceuticals, Inc.
- Product code
- Code KHE
- Device class
- Class 2
- Regulation
- 21 CFR 864.6550
- Advisory panel
- Hematology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
Recent devices under product code KHE
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