The following data is part of a premarket notification filed by Caltag Laboratories, Inc. with the FDA for Caltag Cal-lyse.
Device ID | K965232 |
510k Number | K965232 |
Device Name: | CALTAG CAL-LYSE |
Classification | Counter, Differential Cell |
Applicant | CALTAG LABORATORIES, INC. 605 DILWORTH RD. Downingtown, PA 19335 |
Contact | David C Bishop, Ph.d. |
Correspondent | David C Bishop, Ph.d. CALTAG LABORATORIES, INC. 605 DILWORTH RD. Downingtown, PA 19335 |
Product Code | GKZ |
CFR Regulation Number | 864.5220 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1996-12-31 |
Decision Date | 1997-05-14 |
Summary: | summary |