The following data is part of a premarket notification filed by Welch Allyn, Inc. with the FDA for Pneumocheck W/printer/charger And Accessories.
Device ID | K895253 |
510k Number | K895253 |
Device Name: | PNEUMOCHECK W/PRINTER/CHARGER AND ACCESSORIES |
Classification | Spirometer, Diagnostic |
Applicant | WELCH ALLYN, INC. 4341 STATE ST. RD. P.O. BOX 220 Skaneateles Falls, NY 13153 -0220 |
Contact | John Watkins |
Correspondent | John Watkins WELCH ALLYN, INC. 4341 STATE ST. RD. P.O. BOX 220 Skaneateles Falls, NY 13153 -0220 |
Product Code | BZG |
CFR Regulation Number | 868.1840 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1989-08-21 |
Decision Date | 1989-11-02 |