# K950386: Model 3200P/3200PR Hyperbaric Chamber

- Pathway: 510(k) (Traditional)
- Applicant: Sechrist Industries, Inc.
- Decided: Jun 13, 1995 after 132 days
- Product code: CBF (Chamber, Hyperbaric)
- Device class: 2
- Regulation: 21 CFR 868.5470
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
9 later devices descend from it; 6 cite it directly.
0 of 10 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K993010: Bara-Med, Acrylic Monoplace Hyperbaric Chamber (2000), 3 descendants of its own
- K021693: Pan-America Hyperbarics Hyperbaric Chamber System, Model Pah-S1 (2002), 2 descendants of its own
- K100268: Sechrist Monoplace Hyperbaric Oxygen Chamber (2010), 1 descendant of its own
- K052713: Model 3300E/ER Monoplace Hyperbaric Oxygen Chamber (2005), 1 descendant of its own
- K140559: Sechrist Monoplace Hyperbaric Oxygen Chamber (2014), 0 descendants of its own

Source page: https://510kreport.com/device/K950386
Methodology: https://510kreport.com/methodology