The following data is part of a premarket notification filed by Contour Medical Technology, Inc. with the FDA for Temperature Probe-tp450.
Device ID | K952804 |
510k Number | K952804 |
Device Name: | TEMPERATURE PROBE-TP450 |
Classification | Warmer, Infant Radiant |
Applicant | CONTOUR MEDICAL TECHNOLOGY, INC. 144 SOUTHWAY BLVD. P.O. BOX 397 Lavergne, TN 37086 |
Contact | R. Keith Ferrari |
Correspondent | R. Keith Ferrari CONTOUR MEDICAL TECHNOLOGY, INC. 144 SOUTHWAY BLVD. P.O. BOX 397 Lavergne, TN 37086 |
Product Code | FMT |
CFR Regulation Number | 880.5130 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1995-06-19 |
Decision Date | 1996-04-04 |