510(k) K770614
- Device
- MONITOR, GAS MANIFOLD
- Applicant
- Dynatech Cryomedical Co.
- 510(k) number
- K770614
- Product code
- BXH
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1977-04-07
- Date received
- 1977-03-31
- Regulation
- 868.2610
- Classification name
- Gauge, Gas Pressure, Cylinder/Pipeline
- Medical specialty
- Anesthesiology
- Review panel
- Anesthesiology
- Device class
- 1
- Clearance type
- Traditional
- Third party reviewed
- N
Applicant Contact#
- Address
- 4221 Richmond Rd., NW Walker MI US 49534 49534
FDA Registration Numbers#
- 2518157
- 3038624873
- 2085602
- 9611451
- 3033527731
- 3005273623
- 3005347827
- 9710567
- 3030128613
- 2020813
- 3016734145
Source Documents#
510(k) summary PDF not indicated by FDA