The following data is part of a premarket notification filed by Linvatec Corp. with the FDA for Concept Universal Pump System.
Device ID | K933873 |
510k Number | K933873 |
Device Name: | CONCEPT UNIVERSAL PUMP SYSTEM |
Classification | Insufflator, Hysteroscopic |
Applicant | LINVATEC CORP. 11311 CONCEPT BLVD. Largo, FL 33773 -4908 |
Contact | Martha C Miller |
Correspondent | Martha C Miller LINVATEC CORP. 11311 CONCEPT BLVD. Largo, FL 33773 -4908 |
Product Code | HIG |
CFR Regulation Number | 884.1700 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1993-08-09 |
Decision Date | 1994-12-29 |