Identity
- Trade Name
- Hometa FDA UDI
- Generic Name
- Intravenous gravity infusion monitor FDA UDI
- Device Name
- Drip Assist FDA UDI
- Model / Reference
- G-G10-1A03 FDA UDI
- Description
- Drip Assist FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00850024592070 FDA UDI
- 510(k) Number
- K150687 FDA UDI
- FDA Product Code
- FLN FDA UDI
- GMDN Term
- Intravenous gravity infusion monitor FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.2420 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
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
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
MR Unsafe FDA UDI
Category: Intravenous gravity infusion monitor
Hometa by Hometa, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Intravenous gravity infusion monitor.
- DripAssist — Shift Labs · Class II
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
- Hometa, Inc.
Sources (1)
- FDA UDI 42912ade-85ba-4c27-9a2a-ea9ee32cd26e 35 fields · synced May 31, 2026