Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Porter Instrument Co., Inc. — Predicate Candidate Screening
6 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
156 daysmedian FDA review time
581 days90th percentile
6clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K062155 | DIGITAL MXR-D FLOWMETER | Porter Instrument Co., Inc. | 2006-11-09 | 104 | 1 |
| K981754 | AUTOMATIC VACUUM SWITCH (AVS) MODEL NUMBER AVS 5000 | Porter Instrument Co., Inc. | 1998-06-16 | 29 | 0 |
| K924596 | SES-2012 AUTOMATIC STEAM STERILIZER | Porter Instrument Co., Inc. | 1994-04-15 | 581 | 0 |
| K923781 | MXR-2000 FLOWMETER | Porter Instrument Co., Inc. | 1993-06-10 | 317 | 1 |
| K895638 | STEAM STERILIZER (AUTOCLAVE), DENTAL | Porter Instrument Co., Inc. | 1990-02-22 | 156 | 0 |
| K802067 | CLEAN-AIR POLLUTION REDUCTION SYSTEM | Porter Instrument Co., Inc. | 1980-09-26 | 30 | 0 |
Methodology
Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.
Prepared with Atlas
Predicate research, review-time statistics and recall monitoring for 510(k) teams — atlasbyauro.com/fda