The following data is part of a premarket notification filed by J. H. Emerson Co. with the FDA for Emerson Chest Respirator, Model 33-cre.
Device ID | K881808 |
510k Number | K881808 |
Device Name: | EMERSON CHEST RESPIRATOR, MODEL 33-CRE |
Classification | Ventilator, External Body, Negative Pressure, Adult (cuirass) |
Applicant | J. H. EMERSON CO. 22 COTTAGE PARK AVE. Cambridge, MA 02140 -1691 |
Contact | Emerson, Vp |
Correspondent | Emerson, Vp J. H. EMERSON CO. 22 COTTAGE PARK AVE. Cambridge, MA 02140 -1691 |
Product Code | BYT |
CFR Regulation Number | 868.5935 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1988-04-28 |
Decision Date | 1988-08-04 |