FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
E100M VENTILATOR (E100M)
K Number: K972833
·
Decision Sep 23, 1999
Classifications
1
FEI Numbers
130
Registration Numbers
130
Same Product Code
504
Applicant Total
22
Review Days
785
Research this 510(k) in seconds
The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.
Free to try · every answer cites its records
Basic Information
- Device Name
- E100M VENTILATOR (E100M)
- K Number
- K972833
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 868.5895
- Medical Specialty
- Anesthesiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Newport Medical Instruments, Inc.
- Date Received
- July 30, 1997
- Decision Date
- September 23, 1999
- Product Code
- CBK
- Advisory Committee
- Anesthesiology
- Review Advisory Committee
- AN
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| CBK | Ventilator, Continuous, Facility Use | FDA class 2 | Anesthesiology |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (CBK), ordered by most recent decision date.
Evita (V800); Evita (V600)
FDA 510(k)
FDA Class 2
·Anesthesiology
Inbentus Versatile
FDA 510(k)
FDA Class 2
·Anesthesiology
VPAP Pediatric Face Mask
FDA 510(k)
FDA Class 2
·Anesthesiology
Vivo 45 LS
FDA 510(k)
FDA Class 2
·Anesthesiology
F&P OptiNIV Hospital Vented Full Face Mask Compatible with Single-limb Circuits Size A (ONIV117A); F&P OptiNIV Hospital Vented Full Face Mask Compatible with Single-limb Circuits Size B (ONIV117B); F&P OptiNIV Hospital Vented Full Face Mask Compatible with Single-limb Circuits Size C (ONIV117C); F&P OptiNIV ONIV117-F Hospital Vented Full Face Mask with optional Expiratory Filter Compatible with Single-limb Circuits - Size A (ONIV117A-F); F&P OptiNIV ONIV117-F Hospital Vented Full
FDA 510(k)
FDA Class 2
·Anesthesiology
SV600, SV800 Ventilator
FDA 510(k)
FDA Class 2
·Anesthesiology
Other Clearances by Newport Medical Instruments, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K121891 | NEWPORT AURA VENTILATOR | Nov 9, 2012 | Substantially Equivalent |
| K111146 | NEWPORT HT70 VENTILATOR | Dec 1, 2011 | Substantially Equivalent |
| K101803 | NEWPORT E360 VENTILATOR | Sep 8, 2010 | Substantially Equivalent |
| K090888 | NEWPORT HT70 FAMILY OF VENTILATORS | Nov 18, 2009 | Substantially Equivalent |
| K082724 | NEWPORT HTS50 VENTILATOR WITH DUAL PAC BATTERY SYSTEM | Dec 16, 2008 | Substantially Equivalent |
| K061094 | NEWPORT E500 WAVE VENTILATOR | Jul 28, 2006 | Substantially Equivalent |
| K053502 | NEWPORT E360 VENTILATOR | Jan 10, 2006 | Substantially Equivalent |
| K041082 | NEWPORT NEBSONIC N550 ULTRASONIC NEBULIZER | Sep 7, 2004 | Substantially Equivalent |
| K030780 | NEWPORT E500 WAVE VENTILATOR | Jan 23, 2004 | Substantially Equivalent |
| K992133 | NEWPORT HT50 VENTILATOR WITH HUMIDIFIER HT50-H, NEWPORT HT50 VENTILATOR WITHOUT HUMIDIFIER, HT50-H1, NEWPORT HT50 VENTIL | Aug 4, 2000 | Substantially Equivalent - Subject to Tracking Reg. |