ASPIRATOR
Pump, Portable, Aspiration (manual Or Powered)
WELLS JOHNSON CO.
The following data is part of a premarket notification filed by Wells Johnson Co. with the FDA for Aspirator.
Pre-market Notification Details
| Device ID | K832274 |
| 510k Number | K832274 |
| Device Name: | ASPIRATOR |
| Classification | Pump, Portable, Aspiration (manual Or Powered) |
| Applicant | WELLS JOHNSON CO. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | BTA |
| CFR Regulation Number | 878.4780 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-07-12 |
| Decision Date | 1983-10-20 |
NIH GUDID Devices
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