VENTIPLUS DISPOSABLE MANOMETER 0-60 CM H2O - Ventiplus Disposable Manometer 0-20 Cm H2O
510(k) K102377
Active
Valid until
No expiry
FDA recalls
None foundDocuments
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK102377 | Date18 Nov 2010 | StatusActive |
Recalls
No FDA recalls found in the data synced 22 Oct 2026.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA Product Code
- CAP
- Models / Variants
- Ventiplus Disposable Manometer 0-20 Cm H2O
- Device Class
- Class II
- Regulation
- 21 CFR Part 868.2600
- Advisory Committee
- Anesthesiology
- FDA Decision
- SESE Substantially Equivalent
Overview
AI-generated summary, 6 Oct 2026
The Ventiplus Disposable Manometer is a mechanical pressure monitoring device that measures airway pressure using linear spring compression proportional to gas pressure. It is available in pressure ranges of 0-60 cm H2O and 0-20 cm H2O, with a disposable housing featuring graduated markings for easy reading. This device contains no electronic components, software, or requires an external energy source.
The Ventiplus Disposable Manometer is designed for single patient use and is intended for monitoring airway pressure in clinical settings. It is regulated under FDA 510(k) clearance with product code CAP and is classified as a Monitor, Airway Pressure (includes Gauge And/or Alarm) under regulation 868.2600. The device is supplied in disposable form and requires appropriate storage conditions as specified by the manufacturer.