# K872849: Sperm-Select Additional Indication

- Pathway: 510(k) (Traditional)
- Applicant: Pharmacia, Inc.
- Decided: Sep 28, 1987 after 70 days
- Product code: HDR (Cap, Cervical)
- Device class: 2
- Regulation: 21 CFR 884.5250
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
5 later devices descend from it; 2 cite it directly.
0 of 6 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
- K971809: Isolate (1997), 4 descendants of its own
- K991341: Isolate, Isolate Concentrate, Isolate Stock Solution (1999), 1 descendant of its own
- K980814: Puresperm (1998), 1 descendant of its own
- K023403: Spermgrad, Models 10022/10063 (2002), 0 descendants of its own
- K984172: Modification of Puresperm (1999), 0 descendants of its own

Source page: https://510kreport.com/device/K872849
Methodology: https://510kreport.com/methodology