Atlas FDA

KQW

13 FDA 510(k) clearances · Product code

43 daysmedian time to decision
84 days90th percentile
13clearances measured

FDA profile

Official device name
Goniometer, Nonpowered
Device class
Class I (low risk)
Regulation
21 CFR 888.1520
Medical specialty
Orthopedic
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RecordFirmDate
O'BRIEN GONIOMETER (K926237)Sgarlato Laboratories, Inc.1993-08-02
DOBBHOFF(R) RETRIEVAL FORCEPS (K901744)Biosearch Medical Products, Inc.1990-07-03
THE (CROM) TESTER (K870767)Twin City Surgical, Inc.1987-03-17
HAND HELD GONIOMETER (K850082)Chattanooga Group, Inc.1985-04-04
FINGER BONIOMETER BK7506 (K831550)Fred Sammons, Inc.1983-06-24
THE TELOS EQUIPMENT (K812778)The Telos Co.1981-12-08
UNIVERSAL GONIMETER (K810441)Fred Sammons, Inc.1981-02-27
BK-7497 BULB DYNAMOMETER (K801715)Fred Sammons, Inc.1980-08-04
BK-7505 RADIOPAQUE GONIOMETER, 8 (K801716)Fred Sammons, Inc.1980-08-04
BK-7511 BRASS GONIOMETER (K801717)Fred Sammons, Inc.1980-08-04
BK-7513 STAINLESS STEEL GONIOMETER (K801718)Fred Sammons, Inc.1980-08-04
GONIOMETER, MED. INTER. STAND. BK-7512 (K760301)Fred Sammons, Inc.1976-09-08
GONIOMETER, INTER. STAND. LARGE, BK7514 (K760302)Fred Sammons, Inc.1976-09-08

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Every clearance here is in the API, with alerts when new ones post.