Preceptis Medical, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
5
Inspections
3
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K221254Hummingbird Tympanostomy Tube SystemJuly 27, 2022
K200952Hummingbird Tympanostomy Tube SystemJune 5, 2020
K151830Hummingbird Tympanostomy TubeSeptember 21, 2015
K142282HUMMINGBIRD(TM) TYMPANOSTOMY TUBE SYSTEM (TTS)April 23, 2015
K133921PRECEPTIS TYMPANOSTOMY TUBE INSERTERAugust 22, 2014