The following data is part of a premarket notification filed by Lucas Grason-stadler, Inc. with the FDA for Gsi 37 Auto Tymp.
Device ID | K911095 |
510k Number | K911095 |
Device Name: | GSI 37 AUTO TYMP |
Classification | Tester, Auditory Impedance |
Applicant | LUCAS GRASON-STADLER, INC. 537 GREAT RD. P.O. BOX 1400 Littleton, MA 01460 |
Contact | Janice E Painter |
Correspondent | Janice E Painter LUCAS GRASON-STADLER, INC. 537 GREAT RD. P.O. BOX 1400 Littleton, MA 01460 |
Product Code | ETY |
CFR Regulation Number | 874.1090 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1991-03-13 |
Decision Date | 1991-03-29 |