Andros Analyzers, Inc. FDA Record
Andros Analyzers, Inc. has 0 FDA recalls, 0 inspections, 5 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Andros Analyzers, Inc." is on file.
- Latest 510(k)
- Nov 23, 1990
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 |
|---|---|---|
| K903806 | ANGIOTEC IMAGE MANAGEMENT SYSTEM | Nov 23, 1990 |
| K893476 | ANGIOTEC SPX SPLIT SCREEN DUAL CHANNEL SCAN CONV. | Jun 23, 1989 |
| K892869 | ANGIOTEC ZX DIGITAL IMAGE PROCESSOR | May 26, 1989 |
| K891485 | ANGIOTEC FMX-2220 SYSTEM | May 5, 1989 |
| K852463 | ANDROS ANALYZERS AIRWAY ADAPTER | Jul 8, 1985 |
Andros Analyzers, Inc. and the FDA: common questions
Has Andros Analyzers, Inc. received an FDA warning letter?
No FDA warning letter addressed to the name "Andros Analyzers, Inc." 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 Andros Analyzers, Inc. received an FDA Form 483?
FDA has not published a Form 483 for "Andros Analyzers, Inc." in its reading room. FDA publishes some Form 483s, not all of them.
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