The following data is part of a premarket notification filed by Gi Supply with the FDA for Gi Supply Paracentesis Pump.
Device ID | K970186 |
510k Number | K970186 |
Device Name: | GI SUPPLY PARACENTESIS PUMP |
Classification | Pump, Portable, Aspiration (manual Or Powered) |
Applicant | GI SUPPLY P.O. BOX 289 Willington, CT 06279 |
Contact | Robert G Whalen |
Correspondent | Robert G Whalen GI SUPPLY P.O. BOX 289 Willington, CT 06279 |
Product Code | BTA |
CFR Regulation Number | 878.4780 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1997-01-17 |
Decision Date | 1997-02-14 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
00893029002076 | K970186 | 000 |