The following data is part of a premarket notification filed by L H M Ent., Inc. with the FDA for Single-use, Sterile 4oz Bottle Contain Ster. Water.
Device ID | K901079 |
510k Number | K901079 |
Device Name: | SINGLE-USE, STERILE 4OZ BOTTLE CONTAIN STER. WATER |
Classification | Tube, Tracheostomy (w/wo Connector) |
Applicant | L H M ENT., INC. 855 VIRGINIA AVENUE, P.O. BOX 431 Palm Harbor, FL 34683 |
Contact | Pat Lamb |
Correspondent | Pat Lamb L H M ENT., INC. 855 VIRGINIA AVENUE, P.O. BOX 431 Palm Harbor, FL 34683 |
Product Code | BTO |
CFR Regulation Number | 868.5800 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1990-03-07 |
Decision Date | 1990-05-18 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
B150302964 | K901079 | 000 |
B150302954 | K901079 | 000 |