The following data is part of a premarket notification filed by Shippert Medical Technologies Corp. with the FDA for Expandacell Anatomical Posterior Nasal Pack W/& Without Airway.
Device ID | K955593 |
510k Number | K955593 |
Device Name: | EXPANDACELL ANATOMICAL POSTERIOR NASAL PACK W/& WITHOUT AIRWAY |
Classification | Balloon, Epistaxis |
Applicant | SHIPPERT MEDICAL TECHNOLOGIES CORP. 7002 SOUTH REVERE PARKWAY, SUITE 60 Englewood, CO 80112 |
Contact | Sarah Lake |
Correspondent | Sarah Lake SHIPPERT MEDICAL TECHNOLOGIES CORP. 7002 SOUTH REVERE PARKWAY, 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 | 1995-12-07 |
Decision Date | 1995-12-22 |