FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
AirStrip ONE Web Client with Alarm Communication Management (ACM)
K Number: K211949
·
Decision Dec 9, 2021
Classifications
1
FEI Numbers
72
Registration Numbers
72
Same Product Code
116
Applicant Total
5
Review Days
169
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Basic Information
- Device Name
- AirStrip ONE Web Client with Alarm Communication Management (ACM)
- K Number
- K211949
- Device Class
- FDA class 2
- Clearance Type
- Special
- Regulation Number
- 870.2300
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Airstrip Technologies, Inc.
- Date Received
- June 23, 2021
- Decision Date
- December 9, 2021
- Product Code
- MSX
- Advisory Committee
- Cardiovascular
- Review Advisory Committee
- CV
- 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 |
|---|---|---|---|
| MSX | System, Network And Communication, Physiological Monitors | FDA class 2 | Cardiovascular |
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|---|---|---|---|
| K182226 | AirStrip RPM InvisionHeart Adapter | Sep 11, 2018 | Substantially Equivalent |
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| K143114 | Sense4Baby System Model B+ (MSA) | Mar 10, 2015 | Substantially Equivalent |
| K121712 | AIRSTRIP RPM FOR LIFENET CONSULT | Nov 20, 2012 | Substantially Equivalent |