C-V Monitors Corp. FDA Record
C-V Monitors Corp. has 0 FDA recalls, 0 inspections, 5 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "C-V Monitors Corp." is on file.
- Latest 510(k)
- Oct 26, 1979
Summary
| Records | Count | Last refreshed | Source as of | Status |
|---|---|---|---|---|
| Recalls | 0 | Nov 8, 2026 | File dated Nov 3, 2026 | Current |
| 510(k) clearances | 5 | Nov 8, 2026 | File dated Nov 2, 2026 | Current |
| Inspections | 0 | Nov 14, 2026 | Newest record Nov 5, 2026 | Current |
| Compliance actions | 0 | Nov 2, 2026 | Newest record Oct 29, 2026 | Current |
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Recent 510(k) clearances
| K-Number | Device | Date |
|---|---|---|
| K792099 | 50MM WRITER MODEL CVM 9529 | Oct 26, 1979 |
| K790004 | MONITOR SCOPES, MODELS 9502, 9503 | Feb 28, 1979 |
| K781867 | WRITER, GEMINI-3 | Jan 5, 1979 |
| K780571 | BLOOD PRESSURE MODULE | May 9, 1978 |
| K780572 | DCG PREAMPLIFIER MODULE | May 9, 1978 |
C-V Monitors Corp. and the FDA: common questions
Has C-V Monitors Corp. received an FDA warning letter?
No FDA warning letter addressed to the name "C-V Monitors Corp." is on file. This answer covers that name only: letters addressed to a related company name or to one of its sites are listed on that name's or site's own page.
Has C-V Monitors Corp. received an FDA Form 483?
FDA has not published a Form 483 for "C-V Monitors Corp." in its reading room. FDA publishes some Form 483s, not all of them.
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