# K896120: Schiller Model SP-100 Spirovit (TM)

- Pathway: 510(k) (Traditional)
- Applicant: Schiller America, Inc.
- Decided: Jan 9, 1990 after 77 days
- Product code: BZG (Spirometer, Diagnostic)
- Device class: 2
- Regulation: 21 CFR 868.1840
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
11 later devices descend from it; 1 cites it directly.
0 of 12 devices in its family (counting itself) have a Class I recall.

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

## Most influential descendants
- K984031: Spirovit, Model SP-250 (1999), 10 descendants of its own
- K992823: Spirovit SP-2, Pneumocheck II (2000), 9 descendants of its own
- K022276: Kokomate (2002), 8 descendants of its own
- K051572: Koko Legend (2005), 7 descendants of its own
- K100687: Vitalograph Hand Held Spirometer, Model 2120 (2010), 6 descendants of its own

Source page: https://510kreport.com/device/K896120
Methodology: https://510kreport.com/methodology