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

Cheetah Medical, Inc. · Predicate Candidate Screening

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

90 daysmedian FDA review time

218 days90th percentile

7clearances measured

K-number	Device	Applicant	Decided	Review days	Recalls (K-match)
K103166	CHEETAH RELIANT	Cheetah Medical, Inc.	2011-01-25	90	0
K101487	CHEETAH NICOM SYSTEM	Cheetah Medical, Inc.	2010-07-02	35	0
K083093	CHEETAH RELIANT	Cheetah Medical, Inc.	2008-12-15	59	1
K071631	NICOM ELECTRODES	Cheetah Medical, Inc.	2008-01-18	218	0
K072662	CHEETAH RELIANT, CHEETAH ACTIVE	Cheetah Medical, Inc.	2008-01-16	117	0
K042144	NICOM	Cheetah Medical, Inc.	2004-11-12	95	0
K023370	CHEETAH I.V.D.S., MODEL 2002P	Cheetah Medical, Inc.	2002-12-24	77	0

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