Atlas FDA

REGULATORS, LOW SUCTION

FDA 510(k) clearance K760316 · decided 1976-08-04

Clearance details

K-number
K760316
Device name
REGULATORS, LOW SUCTION
Applicant
Harris-Lake, Inc.
Decision
Substantially Equivalent
Date received
1976-07-26
Decision date
1976-08-04
Days to decision
9 days
Clearance type
Traditional
Product code
KDP
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
BOEHRINGER MRI SUCTION REGULATORY (K013976)Boehringer Laboratories2002-01-08
PM3300 INTERMITTENT VACUUM (K944479)Precision Medical, Inc.1994-12-22
MALCOLM-LYNN(TM) EOT SUCTION REG VALVE(TM) (SRV) ) (K942747)Engineered Orthopedic Technologies, Inc.1994-07-21
BOEHRINGER LABORATORIES SUCTION REGULATOR, MODIFIED (K933232)Boehringer Laboratories1994-03-28
VACUUM POWER BODY FLUID SUCTION APPARATUS (K926140)Hill-Rom, Inc.1993-07-27
PM3000 & PM3100 VACUUM REGULATOR (K922817)Precision Medical, Inc.1993-03-04
OHMEDA CONTINUOUS SUCTION REGULATOR (K883229)Ohmeda Medical1988-10-19
VACUMATE INTERMITTENT/CONTINUOUS CONTROLLER,VM2000 (K875074)Timeter Instrument Corp.1988-02-22
BOEHRINGER LAB SUCTION INTERRUPTER (K853155)Boehringer Laboratories1985-10-16
SUCTION REGULATOR 7700 SERIES (K850200)Boehringer Laboratories1985-03-04
INTERCEPT (K843591)Vital Signs, Inc.1984-10-19
VACUUM REGULATOR 0-2000 MMHG VR-1000 (K834224)Trimeter Instrument Corp.1984-02-27

Recalls involving this device

No recalls on record reference this clearance.