Atlas FDA

MEDILAS LASER

FDA 510(k) clearance K833557 · decided 1984-02-07

Clearance details

K-number
K833557
Device name
MEDILAS LASER
Applicant
Endo Lase, Inc.
Decision
Substantially Equivalent
Date received
1983-10-07
Decision date
1984-02-07
Days to decision
123 days
Clearance type
Traditional
Product code
LNK
Device class
2
Regulation number
878.4810
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
TECHNOMED PULSOLITH 4000 LASER SYSTEM (K925395)Teknomed, Inc.1993-05-21
MDL-2000 LASERTRIPTER (K901723)Candela Laser Corp.1990-07-13
ND:YAG SURGICAL LASER FOR ENDO. GASTRO/URO. APPLI. (K874255)Minnesota Laser Corp.1988-07-12
ND:YAG SURGICAL LASER FOR GASTRO/UROLOGY APPLICA. (K874253)Minnesota Laser Corp.1988-07-12
MODEL 4060 N ND:YAG LASER FOR GASTROENTEROLOGY USE (K880256)Sharplan Lasers, Inc.1988-04-14
MODEL 4060 N ND:YAG LASER FOR UROLOGICAL USE (K880193)Sharplan Lasers, Inc.1988-04-14
ND:YAG 100 SURGICAL LASER FOR GASTRO. AND UROLOGY (K875039)Surgilase, Inc.1988-04-13
MODEL 4900 ND:YAG LASER FOR GASTRO & GENITOUR APPL (K880171)Cooper Lasersonics, Inc.1988-04-11
MODEL 5050 SURGILASER FOR GASTRO-INTESTINAL USE (K871934)Lasermatic, Inc.1988-03-25
MODEL 5050 SURGILASER FOR UROLOGY USE (K871932)Lasermatic, Inc.1988-03-25
SURGI-LIGHT DISPOS.FIBEROPTIC DEL/SYS GI/URO USE (K873892)Laserguide1988-02-02
KTP/532 LASER (K873330)Laserscope1987-11-18

Recalls involving this device

No recalls on record reference this clearance.