The following data is part of a premarket notification filed by Parker Laboratories, Inc. with the FDA for Signapad.
Device ID | K780973 |
510k Number | K780973 |
Device Name: | SIGNAPAD |
Classification | Media, Electroconductive |
Applicant | PARKER LABORATORIES, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | GYB |
CFR Regulation Number | 882.1275 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1978-06-12 |
Decision Date | 1978-07-27 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
10855683006507 | K780973 | 000 |
00855683006272 | K780973 | 000 |
10855683006675 | K780973 | 000 |
10855683006668 | K780973 | 000 |
10855683006651 | K780973 | 000 |
00855683006890 | K780973 | 000 |
00855683006883 | K780973 | 000 |
20855683006917 | K780973 | 000 |
20855683006542 | K780973 | 000 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
SIGNAPAD 88171232 not registered Live/Pending |
ICP Construction, Inc. 2018-10-26 |
SIGNAPAD 73184415 1132043 Live/Registered |
PARKER LABORATORIES, INC. 1978-09-05 |