Atlas FDA

LITHOVAC SUCTION/ASPIRATION PROBE

FDA 510(k) clearance K964111 · decided 1996-12-16

Clearance details

K-number
K964111
Device name
LITHOVAC SUCTION/ASPIRATION PROBE
Applicant
Electro Medical Systems SA
Decision
Substantially Equivalent
Date received
1996-10-15
Decision date
1996-12-16
Days to decision
62 days
Clearance type
Traditional
Product code
KQT
Device class
2
Regulation number
876.4370
Medical specialty
Gastroenterology, Urology
Advisory committee
Gastroenterology, Urology
Location
North Attleboro, MA, 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
EVACUATOR, GASTRO-UROLOGY (K921451)Northgate Technologies, Inc.1992-10-28
EVACUATOR, GASTRO-UROLOGY (K921088)Northgate Technologies, Inc.1992-10-28
CLEANFLOW SYSTEM (K910728)Mitron Technologies, Inc.1991-04-01
VAN-TEC BLADDER EVACUATOR (K880099)Van-Tec, Inc.1988-03-02
BELLA - VAC IRRIGATOR (K874493)Bel-Can Industries1988-02-05
ELLIK EVACUATOR (K860266)R. J. Ltd., Ind.1986-03-05
DOSIMETRIC RELEASE (K830546)American Hospital Supply Corp.1983-05-25
ROSS-EMERSON PUMP, MODEL 55-R (K811779)J. H. Emerson Co.1981-07-13
SUCTION WOUND DRAINAGE DEVICE (K810739)The Urology Group1981-06-26
CATHETER IRRIGATION SYRINGES, #3100,3110 (K801781)The Healthcare Group Laboratories, Inc.1980-08-13
GENERAL PURPOSE IRRIGATING/ASPIR SYR. (K801782)The Healthcare Group Laboratories, Inc.1980-08-13
ELLIK BLADDER EVACUATOR (K800397)Sage Products, Inc.1980-03-10

Recalls involving this device

No recalls on record reference this clearance.