The following data is part of a premarket notification filed by Effner And Spreine Co. with the FDA for Kahn-tact U.s.a., Eff Laryngoscope.
Device ID | K872480 |
510k Number | K872480 |
Device Name: | KAHN-TACT U.S.A., EFF LARYNGOSCOPE |
Classification | Laryngoscope, Rigid |
Applicant | EFFNER AND SPREINE CO. 43 YORKSHIRE WOODS Oak Brook, IL 60521 |
Contact | Gary A Kahn |
Correspondent | Gary A Kahn EFFNER AND SPREINE CO. 43 YORKSHIRE WOODS Oak Brook, IL 60521 |
Product Code | CCW |
CFR Regulation Number | 868.5540 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1987-06-23 |
Decision Date | 1987-08-10 |