Identity
- Trade Name
- CLA® Positive Control Serum FDA UDI
- Generic Name
- Allergen-specific/total immunoglobulin E (IgE) antibody IVD, control FDA UDI
- Device Name
- CLA Pos Ctrl Serum FDA UDI
- Model / Reference
- 93026 FDA UDI
- Description
- CLA Pos Ctrl Serum FDA UDI
Identifiers
- Catalog Number
- 93026 FDA UDI
- Primary DI / UDI-DI
- 00813382010198 FDA UDI
- 510(k) Number
- K910292 FDA UDI
- FDA Product Code
- DHB FDA UDI
- GMDN Term
- Allergen-specific/total immunoglobulin E (IgE) antibody IVD, control FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 866.5750 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Allergen-specific/total immunoglobulin E (IgE) antibody IVD, control
CLA® Positive Control Serum by Minaris Medical America, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Allergen-specific/total immunoglobulin E (IgE) antibody IVD, control.
Cleared under the same submission
K910292 also covers:
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Minaris Medical America, Inc.
Sources (1)
- FDA UDI a42a70b1-90cb-47e0-a028-3f620846f3f0 37 fields · synced May 30, 2026