The following data is part of a premarket notification filed by Polymedco, Inc. with the FDA for Polymedco Oc Auto Micro 80 Fob Test.
Device ID | K041408 |
510k Number | K041408 |
Device Name: | POLYMEDCO OC AUTO MICRO 80 FOB TEST |
Classification | Automated Occult Blood Analyzer |
Applicant | POLYMEDCO, INC. 510 FURNACE DOCK RD. Cortlandt Manor, NY 10567 |
Contact | Helen Landicho |
Correspondent | Helen Landicho POLYMEDCO, INC. 510 FURNACE DOCK RD. Cortlandt Manor, NY 10567 |
Product Code | OOX |
CFR Regulation Number | 864.6550 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2004-05-27 |
Decision Date | 2004-10-21 |