Atlas FDA

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

Minrad, Inc. — Predicate Candidate Screening

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

66 daysmedian FDA review time
106 days90th percentile
14clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K072255MINRAD INC. NASAL SCAVENGING CIRCUITMinrad, Inc.2007-10-18660
K071814LIGHT SABRE SPINAL ACCESS DEVICEMinrad, Inc.2007-10-161060
K062230MR FIBER OPTIC INTUBATING LARYNGOSCOPE HANDLE, SHORT, MODEL Minrad, Inc.2006-08-31290
K062231MR FIBER OPTIC INTUBATING LARYNGOSCOPE HANDLE, STANDARD, MODMinrad, Inc.2006-08-31290
K041852MR TESTED FIBER OPTIC SHORT LARYNGOSCOPE HANDLE, MODEL 31000Minrad, Inc.2004-11-151300
K041846SABRESOURCE DRAPEMinrad, Inc.2004-08-26490
K021084LIGHT SABER SPINAL NEEDLEMinrad, Inc.2002-07-03900
K013040LIGHT SABER INTRODUCER NEEDLEMinrad, Inc.2001-12-07880
K982735LIGHT SABER BONE BIOPSY NEEDLEMinrad, Inc.1998-09-09350
K982018LIGHT SABER ASPIRATION NEEDLEMinrad, Inc.1998-08-07600
K981796LIGHT SABER CORE TISSUE NEEDLEMinrad, Inc.1998-08-05760
K981140MINRAD DRTS LIGHT SABER SYRINGEMinrad, Inc.1998-06-25870
K973067DRTS REMOTE CONTROL DRAPEMinrad, Inc.1997-10-16590
K973073DRTS IMAGE INTENSIFIER DRAPEMinrad, Inc.1997-10-08510

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