Atlas FDA

ELECTRO-SUCTION UNIT

FDA 510(k) clearance K810892 · decided 1981-04-17

Clearance details

K-number
K810892
Device name
ELECTRO-SUCTION UNIT
Applicant
Jedmed Instrument Co.
Decision
Substantially Equivalent
Date received
1981-04-02
Decision date
1981-04-17
Days to decision
15 days
Clearance type
Traditional
Product code
KDQ
Device class
2
Regulation number
880.6740
Medical specialty
General Hospital
Advisory committee
General Hospital
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
EXPRESS CHEST DRAIN (K081718)Atrium Medical Corp.2008-07-25
MILLICORE AB DIGIVENT CHEST DRAINAGE SYSTEM (K062302)Millicore AB2006-10-06
OCEAN CHEST DRAIN (K043582)Atrium Medical Corp.2005-01-21
ATRIUM MEDICAL CORPORATION EXPRESS CHEST DRAIN (K984496)Atrium Medical Corp.1999-05-05
PLEUR-EVAC SAHARA ADULT/PEDIATRIC CHEST DRAINAGE SYSTEM MODEL S-1100, S-1200, 2-2100, AND S-2200 WITH MODEL S-100 AUTOTR (K962856)Deknatel, Inc.1996-08-28
ROCKET PLEURASEAL II CHEST DRAINAGE SYSTEM (K961287)Rocket Medical Plc1996-07-26
MUCUS SPECIMEN TRAP (K962168)Sage Products, Inc.1996-07-22
ATRIUM DRY SUCTION CONTROL WATER SEAL CHEST DRAIN (K950677)Atrium Medical Corp.1995-04-13
PM9000 VAC TRAP (K941818)Precision Medical, Inc.1994-12-12
THORA-KLEX 350 ML PEDIATRIC CHEST DRAINAGE SYSTEM (K932327)Davol, Inc.1993-07-13
ATRIUM 2000 CHEST DRAIN (K912704)Atrium Medical Corp.1991-08-26
PLEUR-EVAC CHEST DRAINAGE SYSTEMS (K905768)Deknatel, Inc.1991-02-11

Recalls involving this device

No recalls on record reference this clearance.