The following data is part of a premarket notification filed by Sps Medical Supply Corp. with the FDA for Airview Bowie Dick; Test Pack, Indicator Sheets.
Device ID | K130211 |
510k Number | K130211 |
Device Name: | AIRVIEW BOWIE DICK; TEST PACK, INDICATOR SHEETS |
Classification | Indicator, Physical/chemical Sterilization Process |
Applicant | SPS MEDICAL SUPPLY CORP. 6789 WEST HENRIETTA RD. Rush, NY 14543 |
Contact | Michael G Nolan |
Correspondent | Michael G Nolan SPS MEDICAL SUPPLY CORP. 6789 WEST HENRIETTA RD. Rush, NY 14543 |
Product Code | JOJ |
CFR Regulation Number | 880.2800 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2013-01-29 |
Decision Date | 2013-07-05 |
Summary: | summary |