Invitrocare Inc
Frederick, MD, US
INVITROCARE INC appears in FDA device records in Frederick, MD. FDA records list 10 510(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 10 510(k) clearances for Invitrocare Inc between 2000 and 2002. The busiest year on record is 2000, with 8. The most recent is 2002, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 2000 | 8 |
| 2001 | 1 |
| 2002 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K023222 | ISOCARE ONE STEP SPERM PROCESSING MEDIUM CAT# 2207-12 | MQL | Substantially Equivalent | |
| K003751 | HYALURONIDASE REAGENT, MODEL CAT#2212 | MQL | Substantially Equivalent | |
| K001967 | PVP-POLYVINYLPYRROLIDONE REAGENT, MODEL CAT#2210 | MQL | Substantially Equivalent | |
| K001113 | IVC THREE BLASTOCYST MEDIUM, CAT # 2007 | MQL | Substantially Equivalent | |
| K000989 | SPERM WASH MEDIUM, CAT# 2003/2005 | MQL | Substantially Equivalent | |
| K993484 | Q-HTF, CAT# 2001 | MQL | Substantially Equivalent | |
| K000938 | IVC ONE MEDIUM | MQL | Substantially Equivalent | |
| K000937 | IVC TWO MEDIUM | MQL | Substantially Equivalent | |
| K000940 | HUMAN SERUM ALBUMIN (HSA) | MQL | Substantially Equivalent | |
| K000939 | HTF-HEPES | MQL | Substantially Equivalent |
Registered establishments
| Registration | FEI | Establishment | Address | Registration expires | Product codes listed |
|---|---|---|---|---|---|
| 3004882774 | 3004882774 | INVITROCARE INC | 8415 Progress Dr Unit F, Frederick, MD 21701 US | 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