The following data is part of a premarket notification filed by Sechrist Industries, Inc. with the FDA for Sechrist Air-oxygen Mixer, 3500/3500hl Series.
| Device ID | K992503 |
| 510k Number | K992503 |
| Device Name: | SECHRIST AIR-OXYGEN MIXER, 3500/3500HL SERIES |
| Classification | Mixer, Breathing Gases, Anesthesia Inhalation |
| Applicant | SECHRIST INDUSTRIES, INC. 4225 EAST LA PALMA Anaheim, CA 92807 |
| Contact | Greg Godfrey |
| Correspondent | Greg Godfrey SECHRIST INDUSTRIES, INC. 4225 EAST LA PALMA Anaheim, CA 92807 |
| Product Code | BZR |
| CFR Regulation Number | 868.5330 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1999-07-27 |
| Decision Date | 1999-08-10 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00852682007323 | K992503 | 000 |
| 00899660002376 | K992503 | 000 |
| 00899660002536 | K992503 | 000 |
| 00899660002543 | K992503 | 000 |
| 00899660002550 | K992503 | 000 |
| 00899660002567 | K992503 | 000 |
| 00899660002574 | K992503 | 000 |
| 00899660002581 | K992503 | 000 |
| 00899660002598 | K992503 | 000 |
| 00899660002604 | K992503 | 000 |
| 00899660002611 | K992503 | 000 |
| 00899660002628 | K992503 | 000 |
| 00899660002635 | K992503 | 000 |
| 00899660002642 | K992503 | 000 |
| 00899660002659 | K992503 | 000 |
| 00899660002369 | K992503 | 000 |