The following data is part of a premarket notification filed by Pymah Corp. with the FDA for Ati Ethylene Oxide Sterilization Indicator.
Device ID | K952995 |
510k Number | K952995 |
Device Name: | ATI ETHYLENE OXIDE STERILIZATION INDICATOR |
Classification | Indicator, Physical/chemical Sterilization Process |
Applicant | PYMAH CORP. 500 ROUTE 202 NORTH Flemington, NJ 08822 -6026 |
Contact | George Levendusky |
Correspondent | George Levendusky PYMAH CORP. 500 ROUTE 202 NORTH Flemington, NJ 08822 -6026 |
Product Code | JOJ |
CFR Regulation Number | 880.2800 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1995-06-28 |
Decision Date | 1996-02-22 |