The following data is part of a premarket notification filed by Baylis Medical Co., Inc. with the FDA for Indiscal Digital Manometer.
| Device ID | K102192 |
| 510k Number | K102192 |
| Device Name: | INDISCAL DIGITAL MANOMETER |
| Classification | Syringe, Piston |
| Applicant | BAYLIS MEDICAL CO., INC. 2645 MATHESON BLVD. E Mississauga, Ontario, CA L4w 5s4 |
| Contact | Meghal Khakhar |
| Correspondent | Meghal Khakhar BAYLIS MEDICAL CO., INC. 2645 MATHESON BLVD. E Mississauga, Ontario, CA L4w 5s4 |
| Product Code | FMF |
| CFR Regulation Number | 880.5860 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2010-08-04 |
| Decision Date | 2011-02-23 |
| Summary: | summary |