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Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account

Medical Technologies of Georgia · Predicate Candidate Screening

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

53 daysmedian FDA review time
146 days90th percentile
12clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K973120READYCATH CATHETERMedical Technologies of Georgia1998-02-251890
K952392MLI SETMedical Technologies of Georgia1995-08-07770
K911129MMG BILE BAGMedical Technologies of Georgia1991-08-071460
K873136MMG CATH-N-PLACEMedical Technologies of Georgia1987-09-09300
K871949MMG DELEE SUCTION CATHETER W/MUCOUS TRAPMedical Technologies of Georgia1987-06-15260
K854821MMG EXTERNAL FEMALE CATHETERSMedical Technologies of Georgia1986-04-241420
K854660THE MMG ENTERAL FEEDING ADMINISTRATION SETMedical Technologies of Georgia1986-01-21620
K840839MMG FOLEY CATHETERMedical Technologies of Georgia1984-04-17530
K840897OXYGEN TUBINGMedical Technologies of Georgia1984-03-16180
K821853U-100 BAGMedical Technologies of Georgia1982-07-22290
K821854U-200 BAGMedical Technologies of Georgia1982-07-22290
K780037EXERCISER, RESP., DEEP BREATHINGMedical Technologies of Georgia1978-02-24460

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