Atlas FDA

SCHNEIDER-SHILEY PRESSURE MANOMETER

FDA 510(k) clearance K861605 · decided 1986-05-28

Clearance details

K-number
K861605
Device name
SCHNEIDER-SHILEY PRESSURE MANOMETER
Applicant
Shiley, Inc.
Decision
Substantially Equivalent
Date received
1986-04-29
Decision date
1986-05-28
Days to decision
29 days
Clearance type
Traditional
Product code
KRK
Device class
2
Regulation number
870.1140
Medical specialty
Cardiovascular
Advisory committee
Cardiovascular
Location
Irvine, CA, 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
UST-5268P-5 TRANSDUCER (K950607)Aloka Co., Ltd.1995-09-15
CENTRAL VENOUS PRESSURE MANOMETER (K904674)Medex, Inc.1990-12-27
ADMINISTRATION/MANOMETER SET W/3 WAY STOPCOCK (K884386)Ethitek Pharmaceuticals Co.1989-01-05
MODIFIED SCHNEIDER-SHILEY PRESSURE MANOMETER (K875322)Schneider-Shilley (Usa)1988-03-28
MANOMETER SET C.V.P. #S 298/299 (K830910)Exco, Inc.1983-04-05
MEDIFIX (K813498)Burron Medical Products, Inc.1982-01-07
MEDIFIX GRADUATED SCALE (K813195)Burron Medical Products, Inc.1981-12-29
VENOUS PRESSURE MONITOR, MF 35 LF (K790668)Deco Medical, Inc.1979-05-23

Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
BJORK-SHILEY CARDIAC VALVE (P780008/S013)Shiley, Inc.1986-10-31
BJORK-SHILEY CARDIAC VALVE (P780008/S014)Shiley, Inc.1985-04-09
BJORK-SHILEY CARDIAC VALVE (P780008/S015)Shiley, Inc.1984-11-26
BJORK-SHILEY CARDIAC VALVE (P780008/S011)Shiley, Inc.1984-05-15
BJORK-SHILEY CARDIAC VALVE (P780008/S007)Shiley, Inc.1983-05-20
BJORK-SHILEY CARDIAC VALVE (P780008/S005)Shiley, Inc.1982-02-05