Atlas FDA

ELLIK BLADDER EVACUATOR

FDA 510(k) clearance K800397 · decided 1980-03-10

Clearance details

K-number
K800397
Device name
ELLIK BLADDER EVACUATOR
Applicant
Sage Products, Inc.
Decision
Substantially Equivalent
Date received
1980-02-26
Decision date
1980-03-10
Days to decision
13 days
Clearance type
Traditional
Product code
KQT
Device class
2
Regulation number
876.4370
Medical specialty
Gastroenterology, Urology
Advisory committee
Gastroenterology, Urology
Location
Mchenry, IL, US
Third-party review
No
Expedited review
No

+ Add to Predicate Builder ◉ Watch Sage Products

Need this as data, not a web page?

Query all 176,000+ clearances through the Atlas FDA API, or subscribe to weekly change alerts. Self-serve from $29/mo.

Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
LITHOVAC SUCTION/ASPIRATION PROBE (K964111)Electro Medical Systems SA1996-12-16
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

Recalls involving this device

No recalls on record reference this clearance.