Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Dayspring Medical, Inc. with 5 510(k) clearances. The most recent is a 510(k) clearance dated Jun 22, 1999: VENTED DIAKYSATE PORT CCAP, RED PLIABLE VINYL - DAYSPRING MEDICAL PART NO, DPC101VS.
| Jun 22, 1999 | VENTED DIAKYSATE PORT CCAP, RED PLIABLE VINYL - DAYSPRING MEDICAL PART NO, DPC101VSK991005 · LLB | 510(k) clearances |
| Jun 9, 1999 | PUMP SEGMENT RINSE LINE W/ SLIP-ON CONNECTOR, PUMP SEGMENT RINSE LINE W/ LUER-LOCK CONNECTOR, T-CONNECTOR, SHORT, W/ SLIK991003 · FKY | 510(k) clearances |
| Sep 12, 1996 | BLLOD PORT CAP, DIALYSATE PORT CAP, VENTED DIALYSATE PORT CAP WITH RED PLIABLE VINYLK961039 · FJI | 510(k) clearances |
| Jun 11, 1996 | BLOOD PORT CAP, DIALYSATE PORT CAP, RED HARD PLASTICK961040 · FJI | 510(k) clearances |
| Jun 10, 1996 | BLOOD PORT CAP, LUER-LOCK FITTING, DAYSPRING MEDICAL PART NO. BPC252LLK961026 · FJI | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
