The following data is part of a premarket notification filed by United Medical Industries Co. Ltd. with the FDA for Unicryl M.
Device ID | K042285 |
510k Number | K042285 |
Device Name: | UNICRYL M |
Classification | Suture, Surgical, Absorbable, Polydioxanone |
Applicant | UNITED MEDICAL INDUSTRIES CO. LTD. 3RD INDUSTRIAL CITY SANAYYA, OPPOSITE TO OBAIKAN Riyadh, Central Province, SA 11553 |
Contact | Mohammed Azeez |
Correspondent | Mohammed Azeez UNITED MEDICAL INDUSTRIES CO. LTD. 3RD INDUSTRIAL CITY SANAYYA, OPPOSITE TO OBAIKAN Riyadh, Central Province, SA 11553 |
Product Code | NEW |
CFR Regulation Number | 878.4840 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2004-08-24 |
Decision Date | 2004-12-10 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
06285379148841 | K042285 | 000 |