The following data is part of a premarket notification filed by J. H. Emerson Co. with the FDA for Emerson Thoracic Suction Reg. #55-jp.
| Device ID | K820077 |
| 510k Number | K820077 |
| Device Name: | EMERSON THORACIC SUCTION REG. #55-JP |
| Classification | Regulator, Vacuum |
| Applicant | J. H. EMERSON CO. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | KDP |
| CFR Regulation Number | 880.6740 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-01-12 |
| Decision Date | 1982-01-28 |