FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
BO MED BIA
K Number: K811999
·
Decision Aug 31, 1981
Classifications
1
FEI Numbers
69
Registration Numbers
69
Same Product Code
113
Applicant Total
8
Review Days
51
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Basic Information
- Device Name
- BO MED BIA
- K Number
- K811999
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 870.2770
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Applicant
- Bomed Medical Mfr., Ltd.
- Date Received
- July 11, 1981
- Decision Date
- August 31, 1981
- Product Code
- DSB
- 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 |
|---|---|---|---|
| DSB | Plethysmograph, Impedance | FDA class 2 | Cardiovascular |
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Other Clearances by Bomed Medical Mfr., Ltd.
| K Number | Device Name | ||
|---|---|---|---|
| K853706 | BOMED-CDM | Apr 14, 1986 | Substantially Equivalent |
| K853705 | BOMED-EEA | Jan 13, 1986 | Substantially Equivalent |
| K831422 | BIOFLOW | Sep 12, 1983 | Substantially Equivalent |
| K831421 | BOMED BIOCON | Sep 12, 1983 | Substantially Equivalent |
| K830792 | PULSETTE 110 TRANSCUTANEOUS ELEC-NERVE | Mar 29, 1983 | Substantially Equivalent |
| K813020 | BOMED-NCCOM | Dec 14, 1981 | Substantially Equivalent |
| K810064 | PULSARII, HIGH VOLT. GALVANIC MUSC. STIM | Jan 26, 1981 | Substantially Equivalent |