The following data is part of a premarket notification filed by Med-tech Develoment Corp. with the FDA for Maklakov Style Tonometer.
Device ID | K860330 |
510k Number | K860330 |
Device Name: | MAKLAKOV STYLE TONOMETER |
Classification | Tonometer, Manual |
Applicant | MED-TECH DEVELOMENT CORP. 11300 49TH ST. NORTH Clearwater, FL 33520 |
Contact | Jose H Bedoya |
Correspondent | Jose H Bedoya MED-TECH DEVELOMENT CORP. 11300 49TH ST. NORTH Clearwater, FL 33520 |
Product Code | HKY |
CFR Regulation Number | 886.1930 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1986-01-29 |
Decision Date | 1986-02-12 |