Identity
- Trade Name
- Good Neighbor FDA UDI
- Generic Name
- Aneroid manual sphygmomanometer FDA UDI
- Device Name
- Good Neighbor Self-Taking Home Blood Pressure Kit With Attached Stethoscope, Adult FDA UDI
- Model / Reference
- 90-5501 FDA UDI
- Description
- Good Neighbor Self-Taking Home Blood Pressure Kit With Attached Stethoscope, Adult FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00087701429989 FDA UDI
- 510(k) Number
- K222652 FDA UDI
- FDA Product Code
- DXQ FDA UDI
- GMDN Term
- Aneroid manual sphygmomanometer FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.1120 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
Yes
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
Yes
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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Aneroid manual sphygmomanometer
Good Neighbor by Amerisourcebergen Drug Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Aneroid manual sphygmomanometer.
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- Princess — American Diagnostic Corporation · Class II
- Diagnostix™ — American Diagnostic Corporation · Class II
- E-sphyg™ — American Diagnostic Corporation · Class II
- BAUM — W.A. BAUM CO., INC. · Class II
Cleared under the same submission
K222652 also covers:
- HCS — Concordance Healthcare Solutions LLC
- HCS — Concordance Healthcare Solutions LLC
- HCS — Concordance Healthcare Solutions LLC
- HCS — Concordance Healthcare Solutions LLC
- HealthSmart — DMS HOLDINGS, INC.,
- MABIS — DMS HOLDINGS, INC.,
- MABIS — DMS HOLDINGS, INC.,
- MABIS — DMS HOLDINGS, INC.,
- VERIDIAN — VERIDIAN HEALTHCARE
- VERIDIAN — VERIDIAN HEALTHCARE
- Veridian Healthcare — VERIDIAN HEALTHCARE
- Veridian Healthcare — VERIDIAN HEALTHCARE
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
- Amerisourcebergen Drug Corporation
Sources (1)
- FDA UDI 2644103b-7636-4aed-b9de-fc5285ed5e58 34 fields · synced May 31, 2026