Endocare, Inc.
Endocare, Inc. holds FDA 510(k) medical device clearances, first cleared 1996, most recent 2010.
Top product codes for Endocare, Inc.
Recent clearances by Endocare, Inc.
- K101333 — CRYOCARE CS SURGICAL SYSTEM
- K062175 — CRYOCARE CN2 SYSTEM
- K060279 — CRYOCARE CS SURGICAL SYSTEM
- K050347 — MODIFICATION TO CRYOCARE CS SURGICAL SYSTEM
- K032333 — CRYOCARE CS SURGICAL SYSTEM
- K023757 — CRYOCARE SURGICAL SYSTEM, MODEL CRYO 20
- K021010 — MODIFIED CARDIAC CRYOSURGICAL SYSTEM, MODELS 6TCS1 & 6TCSE
- K020082 — ERECAID CLASSIC SYSTEM; ERECAID ESTEEM MANUAL SYSTEM; ERECAID ESTEEM BATTERY SYSTEM
- K011074 — CRYOCARE SURGICAL SYSTEM
- K003811 — CRYOCARE SURGICAL SYSTEM
- K011040 — CRYOCARE CARDIAC SURGICAL SYSTEM
- K003528 — SANARUS CORE TISSUE BIOPSY SYSTEM
- K010339 — ENDOCARE PERCUTANEOUS ACCESS SET
- K002615 — SURGICAL SYSTEM WITH CRYOGUIDE
- K002396 — ENDOCARE PERCUTANEOUS ACCESS SET
- K980110 — ENDOCRE CRYOCARE CRYOSURGICAL SYSTEM
- K973686 — ENDOCARE CRYOCARE CRYOSURGICAL SYSTEM
- K963970 — ENDOCARE CRYOCARE CRYOSURGICAL SYSTEM URETHRAL WARMING SYSTEM
- K965118 — ENDOCARE MONOPOLAR ELECTRODE
- K965243 — ENDOCARE ELECTROSURGICAL ELECTRODE
- K963826 — ENDOCARE CRYCARE CRYOSURGICAL SYSTEM
- K961365 — ENDOCARE ELECTORNIC THERMOMETER SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.