FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
AMBU SINGLE PATIENT USE PEEP VALVE
K Number: K923976
·
Decision Jan 5, 1993
Classifications
1
FEI Numbers
71
Registration Numbers
72
Same Product Code
79
Applicant Total
33
Review Days
151
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Basic Information
- Device Name
- AMBU SINGLE PATIENT USE PEEP VALVE
- K Number
- K923976
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 868.5965
- Medical Specialty
- Anesthesiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Ambu, Inc.
- Date Received
- August 7, 1992
- Decision Date
- January 5, 1993
- Product Code
- BYE
- 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 |
|---|---|---|---|
| BYE | Attachment, Breathing, Positive End Expiratory Pressure | FDA class 2 | Anesthesiology |
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|---|---|---|---|
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| K042843 | AMBU SPUR II INFANT AND PEDIATRIC SINGLE PATIENT USE RESUSCITATORS | Nov 12, 2004 | Substantially Equivalent |
| K041734 | AMBU DISPOSABLE ECG ELECTRODE | Sep 22, 2004 | Substantially Equivalent |
| K040991 | AMBU DISPOSABLE PRESSURE MANOMETER | Jul 22, 2004 | Substantially Equivalent |
| K041026 | AMBU BLUE SENSOR, MRX, ECG ELECTRODE PRODUCT #:MRX-00-S | Jun 28, 2004 | Substantially Equivalent |
| K032278 | AMBU NEUROLINE SINGLE PATIENT EEG/EP CUP ELECTRODE | Mar 5, 2004 | Substantially Equivalent |
| K032421 | AMBU PEDIATRIC MULTI-FUNCTION DEFIBRILLATION ELECTRODE | Feb 27, 2004 | Substantially Equivalent |
| K010583 | AMBU GEL, HYDROGEL BURN DRESSING | May 25, 2001 | Substantially Equivalent |
| K993278 | AMBU NEONATE SILICONE RESUSCITATOR | May 17, 2000 | Substantially Equivalent |