Atlas FDA

MANOMETER SET C.V.P. #S 298/299

FDA 510(k) clearance K830910 · decided 1983-04-05

Clearance details

K-number
K830910
Device name
MANOMETER SET C.V.P. #S 298/299
Applicant
Exco, Inc.
Decision
Substantially Equivalent
Date received
1983-03-21
Decision date
1983-04-05
Days to decision
15 days
Clearance type
Traditional
Product code
KRK
Device class
2
Regulation number
870.1140
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
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
SCHNEIDER-SHILEY PRESSURE MANOMETER (K861605)Shiley, Inc.1986-05-28
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.