FDA product code IDW: Dispensers, Paraffin
IDW is the FDA product code for dispensers, paraffin. It is a Class I device, regulated under 21 CFR 864.3010 and reviewed by the Pathology panel. FDA has cleared 1 510(k) submission under IDW. The average 510(k) review took 34 days (median 34). FDA has posted 1 recall for IDW devices, 1 initiated in the last five years.
Classification
| Field | Value |
|---|---|
| Device name | Dispensers, Paraffin |
| Device class | Class I |
| Regulation | 21 CFR 864.3010 |
| Review panel | PA — Pathology |
| Medical specialty | Pathology |
| Premarket route | 510(k) exempt |
| GMP exempt | Yes |
Compare with all 510(k) review times · Search every IDW clearance
Top IDW applicants
| Applicant | Clearances | Latest |
|---|---|---|
| Thermolyne Corp. | 1 | 1979-11-20 |
Most recent IDW clearances
| 510(k) | Applicant | Device | Decision date | Review days |
|---|---|---|---|---|
| K792095 | Thermolyne Corp. | HISTO-CENTER II | 1979-11-20 | 34 |
Recalls for IDW devices
1 product recalls in 1 recall events; 1 initiated in the last five years and 1 still open. Most recent: 2024-05-10.
| Year | Recalls |
|---|---|
| 2024 | 1 |
Frequently asked questions
What is FDA product code IDW?
IDW is the FDA product code for dispensers, paraffin. It is a Class I device, regulated under 21 CFR 864.3010 and reviewed by the Pathology panel.
What device class is IDW?
Class I, regulation 21 CFR 864.3010. Typical premarket route: 510(k) exempt.
How long does a 510(k) take for product code IDW?
Across 1 cleared submissions the average was 34 days from receipt to decision (median 34).
Which companies have the most IDW clearances?
Thermolyne Corp. (1).
Have IDW devices been recalled?
Yes: 1 product recalls across 1 recall events; the most recent began 2024-05-10.
Next steps
- Run an FDA pathway report with predicate devices for product code IDW
- Run a recall and safety report across every IDW manufacturer
- Watch product code IDW for new clearances and recalls
Source: openFDA device classification, 510(k), PMA, De Novo and recall data (public domain). Review days run from FDA receipt to decision. Not regulatory advice.
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