The following data is part of a premarket notification filed by Southmedic, Inc. with the FDA for Anaeslock Three Vaporizer Interlock Hva003.
| Device ID | K843993 |
| 510k Number | K843993 |
| Device Name: | ANAESLOCK THREE VAPORIZER INTERLOCK HVA003 |
| Classification | Vaporizer, Anesthesia, Non-heated |
| Applicant | SOUTHMEDIC, INC. P.O. BOX 7278 Ancaster, Ontario, CA |
| Contact | Lee Mcdonald |
| Correspondent | Lee Mcdonald SOUTHMEDIC, INC. P.O. BOX 7278 Ancaster, Ontario, CA |
| Product Code | CAD |
| CFR Regulation Number | 868.5880 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1984-10-11 |
| Decision Date | 1984-11-15 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 10620974001956 | K843993 | 000 |
| 10620974001888 | K843993 | 000 |