The following data is part of a premarket notification filed by Lake Medical Products, Inc. with the FDA for Lake Disposable Probe Cover.
Device ID | K880578 |
510k Number | K880578 |
Device Name: | LAKE DISPOSABLE PROBE COVER |
Classification | Thermometer, Electronic, Clinical |
Applicant | LAKE MEDICAL PRODUCTS, INC. 11866 ADIE RD. Maryland Heights, MO 63043 |
Contact | Eli Schachet |
Correspondent | Eli Schachet LAKE MEDICAL PRODUCTS, INC. 11866 ADIE RD. Maryland Heights, MO 63043 |
Product Code | FLL |
CFR Regulation Number | 880.2910 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1988-02-10 |
Decision Date | 1988-03-31 |