Grownsy BC023
Grownsy BC023 is a Class II device made by Oak Tech LLC, listed in FDA GUDID since 25 Apr 2024 (UDI-DI 00747976833422), registry data as of 23 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00747976833422 | Date25 Apr 2024 | StatusListed |
Official records
- AccessGUDID record 00747976833422
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Grownsy
- Generic name
- Nasal aspirator, electric
- Model / reference
- BC023
- Primary DI / UDI-DI
- 00747976833422
- FDA product code
- KDQ
- GMDN term
- Nasal aspirator, electric
- Device class
- Class II
- Regulation number
- 880.6740
- GUDID distribution status
- In Commercial Distribution
Similar devices
Other devices filed under FDA product code KDQ (Bottle, Collection, Vacuum).
- One-Vac™ 00884450749609 EVAC1000/A by Merit Medical Systems, Inc.
- MUCUS SPECIMEN TRAP by SAGE PRODUCTS LLC
- PLEURAL DRAINAGE SYSTEM #PDS-4300 by Bentley Laboratories, Inc.
- NIFA NON INVASIVE FLUTTER ASSEMBLY by Emergency Management Products, Inc.
- VAC-RITE by Medical Development Co.
- BARD PARKER THORACIC VENT by Bd Becton Dickinson Vacutainer Systems Preanalytic
- 710202 by US Endoscopy
- OCEAN CHEST DRAIN by Atrium Medical Corp.
- Thora-Vent Thoracic Vent TV11-10 by Uresil Corp.
- THORA-DRAIN III PLASTIC DRAINAGE SYSTEM by Chesebrough-Pond'S U.S.A. Co.