The following data is part of a premarket notification filed by Shippert Medical Technologies Corp. with the FDA for Expandacell Injecto-pak Nasal Pack.
Device ID | K954845 |
510k Number | K954845 |
Device Name: | EXPANDACELL INJECTO-PAK NASAL PACK |
Classification | Balloon, Epistaxis |
Applicant | SHIPPERT MEDICAL TECHNOLOGIES CORP. 7002 SOUTH REVERE PKWY. SUITE 60 Englewood, CO 80112 |
Contact | Sarah M Lake |
Correspondent | Sarah M Lake SHIPPERT MEDICAL TECHNOLOGIES CORP. 7002 SOUTH REVERE PKWY. SUITE 60 Englewood, CO 80112 |
Product Code | EMX |
CFR Regulation Number | 874.4100 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1995-10-23 |
Decision Date | 1995-11-27 |