Atlas FDA

SURGICAL LIGHT

FDA 510(k) clearance K823360 · decided 1982-12-03

Clearance details

K-number
K823360
Device name
SURGICAL LIGHT
Applicant
Amsco Co.
Decision
Substantially Equivalent
Date received
1982-11-05
Decision date
1982-12-03
Days to decision
28 days
Clearance type
Traditional
Product code
FTD
Device class
2
Regulation number
878.4580
Medical specialty
General, Plastic Surgery
Advisory committee
General, Plastic Surgery
Location
Walker, MI, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
SCINTILLANT DUAL BENT TIP SURGICAL LIGHT, SCINTILLANT DUAL STRAIGHT TIP SURGICAL LIGHT (K133425)Engineered Medical Solutions Co., LLC2013-12-05
VOLISTA 400; VOLISTA 600 (K130513)Maquet S.A.S.2013-05-08
POLARIS 100/200 (K123776)Drager Medical GmbH2013-03-08
ATRICURE DISSECTOR (K111020)AtriCure, Inc.2011-06-09
HM-LAMP II (K100234)Hillusa, Inc.2010-07-08
STRYKER KNIFELIGHT (K100884)Howmedica Osteonics Corp.2010-06-25
SCINTILLANT SURGICAL LIGHT, MODEL 2644-01-0001 (K071180)Engineered Medical Solutions Co., LLC2007-06-20
HALUX IRIS EXAMINATION AND SURGICAL LAMP (K053364)Waldmann Lighting2006-02-23
ATRICURE DISSECTOR (K041681)AtriCure, Inc.2004-07-01
AMSCO HARMONY SURGICAL LIGHTING AND MEDIA SYSTEM (K013242)STERIS Corporation2001-12-13
SOLA 700,SOLA 500, SOLA 300 (K010724)Drager Medizintechnik GmbH2001-06-07
ST. FRANCIS OPERATING THEATRE LAMP, MODELS OLH01-125 AND LC-055 (K003423)St. Francis Medical Equipment Co., Ltd.2001-02-22

Recalls involving this device

No recalls on record reference this clearance.