Atlas FDA

Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account

Snyder Laboratories, Inc. — Predicate Candidate Screening

16 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.

43 daysmedian FDA review time
63 days90th percentile
16clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K843906SNYDER HEMOVAC WOUND DRAINAGE DEVICESSnyder Laboratories, Inc.1984-11-05330
K821321SNYDER DEBRIBEMENT SYSTEM LDP-1Snyder Laboratories, Inc.1982-08-06940
K800861SNYDER HEMOVAC CHEST DRAINAGE SOLUTIONSnyder Laboratories, Inc.1980-05-02160
K800577SNYDER HEMOVAC TM VENTED WOUND KITSnyder Laboratories, Inc.1980-04-16330
K800543SNYDER HYSTERECTOMY Y TUBE KITSnyder Laboratories, Inc.1980-04-16370
K800578SURGIVAC TMSnyder Laboratories, Inc.1980-04-16330
K800542100 ML SNYDER HEMOVACSnyder Laboratories, Inc.1980-04-02230
K790607GREENLINE IRRIGATION TRAYSSnyder Laboratories, Inc.1979-05-11430
K790420SUCTION CONNECTING TUBINGSnyder Laboratories, Inc.1979-04-23540
K790419YANKAUER & POODLE SUCTION INSTRUMENTSSnyder Laboratories, Inc.1979-04-23540
K790606CATHETERS, GREENLINE SUCTIONSnyder Laboratories, Inc.1979-04-23250
K790254FOLEY CATHETERIZATION TRAYSnyder Laboratories, Inc.1979-04-10630
K790253URINARY DRAINAGE BAGSnyder Laboratories, Inc.1979-04-10630
K790271TRAY AND BAG, CATHETERIZATIONSnyder Laboratories, Inc.1979-03-06560
K790272TRAY, URETHRAL CATHETERIZATIONSnyder Laboratories, Inc.1979-03-06520
K781400HEMOVAC TUBING MATERIAL CHANGESnyder Laboratories, Inc.1978-09-20360

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