The following data is part of a premarket notification filed by Quantum Instruments Corp. with the FDA for Quantum Mono-polar Electrosurgical Cable.
Device ID | K941908 |
510k Number | K941908 |
Device Name: | QUANTUM MONO-POLAR ELECTROSURGICAL CABLE |
Classification | Electrosurgical, Cutting & Coagulation & Accessories |
Applicant | QUANTUM INSTRUMENTS CORP. 17304 PRESTON RD. SUITE 1035 Dallas, TX 75252 |
Contact | M. J Ward |
Correspondent | M. J Ward QUANTUM INSTRUMENTS CORP. 17304 PRESTON RD. SUITE 1035 Dallas, TX 75252 |
Product Code | GEI |
CFR Regulation Number | 878.4400 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1994-04-19 |
Decision Date | 1994-05-23 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
B150QI10040 | K941908 | 000 |
B1502500400122 | K941908 | 000 |
B1502500400124 | K941908 | 000 |
B15026006MD2 | K941908 | 000 |
B15026006MD4 | K941908 | 000 |
B150277KAD2 | K941908 | 000 |
B150277KAD4 | K941908 | 000 |
B150277KBD2 | K941908 | 000 |
B150277KBD4 | K941908 | 000 |
B150QD10012 | K941908 | 000 |
B150QD10014 | K941908 | 000 |
B150QD10042 | K941908 | 000 |
B150QD10044 | K941908 | 000 |
B150QI10010 | K941908 | 000 |
B150QI10030 | K941908 | 000 |
B1502500400110 | K941908 | 000 |