510(k) K934367
- Device
- Pc-mini
- Applicant
- GE MEDICAL SYSTEMS
- 510(k) number
- K934367
- Product code
- JYD
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1993-11-08
- Date received
- 1993-09-07
- Regulation
- 878.4800
- Classification name
- Chisel, Mastoid
- Medical specialty
- General, Plastic Surgery
- Review panel
- General, Plastic Surgery
- Device class
- 1
- Clearance type
- Traditional
- Statement or summary
- Summary
- Third party reviewed
- No
Applicant Contact#
- Contact
- LARRY A KROGER
- Address
- P.O. Box 414 Milwaukee WI US 53201 53201
FDA Registration Numbers#
- 3002949614
- 8030607
- 9613926
- 3013576617
- 9616246
- 3014314623
- 3007597038
- 3005809810
- 9611278
- 3035708926
- 3011137372
- 9611283
- 3014615697
- 1926681
- 8010155
- 3010041511
- 3003418325
- 8040278
- 1836161
- 3005067367
- 3011110913
- 3014334038
- 3005528784
- 3003244954