Shandong Intco Medical Products Co Ltd
Qingzhou Shandong, CN
SHANDONG INTCO MEDICAL PRODUCTS CO LTD appears in FDA device records in Qingzhou Shandong, CN. FDA records list 4 510(k) clearances between and , no PMA records and one registered establishment. As of , FDA records show no recalls for this company, and at least one establishment registration is current.
FDA records held for this company
510(k) clearance history
FDA records hold 4 510(k) clearances for Shandong Intco Medical Products Co Ltd between 2022 and 2023. The busiest year on record is 2023, with 3. The most recent is 2023, with 3.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 2022 | 1 |
| 2023 | 3 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K233042 | Sterile Nitrile Examination Gloves Powder Free Tested for Use with Chemotherapy Drugs and Fentanyl Citrate | LZA | Substantially Equivalent | |
| K231408 | Basic Synguard Nitrile Exam Gloves, Powder Free, Blue Colored, Non-Sterile | LZA | Substantially Equivalent | |
| K223298 | Sterile Latex Examination Gloves Powder Free (S, M, L, Extra L) | LYY | Substantially Equivalent | |
| K213509 | Latex Examination Gloves, Powder Free | LYY | Substantially Equivalent |
Registered establishments
| Registration | FEI | Establishment | Address | Registration expires | Product codes listed |
|---|---|---|---|---|---|
| 3011391433 | 3011391433 | SHANDONG INTCO MEDICAL PRODUCTS CO LTD | 9888 Qiwang Road, Qingzhou Shandong 262500 CN | 2026 |
Registration numbers link to the FDA registration and listing record for that establishment.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain