Atlas FDA

OHIO DISPOSABLE CLEAR SUCTION INSTRUMENT

FDA 510(k) clearance K801641 · decided 1980-07-28

Clearance details

K-number
K801641
Device name
OHIO DISPOSABLE CLEAR SUCTION INSTRUMENT
Applicant
Ohio Medical Products
Decision
Substantially Equivalent
Date received
1980-07-17
Decision date
1980-07-28
Days to decision
11 days
Clearance type
Traditional
Product code
DTS
Device class
2
Regulation number
870.4420
Medical specialty
Cardiovascular
Advisory committee
Cardiovascular
Location
Mchenry, IL, 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
ESTECH CLEARVIEW MV ATRIAL DEPRESSOR (K053021)Estech, Inc.2006-01-26
CALIFORNIA MEDICAL LABORATORIES INC. STANDARD AND SMALL RIGID TIP SUCTION WANDS (K982891)California Medical Laboratories, Inc.1998-09-30
IBC CARDIAC SUCTION WARD (K963756)International Biophysics Corp.1997-11-14
FLEXIBLE INTRACARDIAC SUCTION DEVICE (K905008)Gish Biomedical, Inc.1991-01-23
HAND-HELD INTRACARDIAC SUCKERS W/ERGONOMIC HANDLES (K900339)Shiley, Inc.1990-03-28
ROBICSEK INTRACARDIAC SUCTION WAND (K891906)Gish Biomedical, Inc.1989-06-13
DISPOSABLE SUCKER SYSTEM (K801400)Texas Medical Products, Inc.1980-06-30
DISPOSSABLE SUCTION TUBE, 6 FRENCH (K791846)Dlp, Inc.1979-10-02

Recalls involving this device

No recalls on record reference this clearance.