Atlas FDA

E-Z LOOP

FDA 510(k) clearance K870577 · decided 1987-04-17

Clearance details

K-number
K870577
Device name
E-Z LOOP
Applicant
John F. Greer Co., Inc.
Decision
Substantially Equivalent
Date received
1987-02-10
Decision date
1987-04-17
Days to decision
66 days
Clearance type
Traditional
Product code
EXB
Device class
1
Regulation number
876.5900
Medical specialty
Gastroenterology, Urology
Advisory committee
Gastroenterology, Urology
Location
Oakland, CA, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

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RecordFirmDate
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LAKE OSTOMY CARE SET (K922730)Lake Medical Products, Inc.1993-12-30
ODOR-END EMERGENCY CLEAN UP POWDER (K882878)Cdc Products Corp.1988-12-08
CONSEAL COLOSTOMY CONTINENCE SYSTEM (ONE-PIECE) (K881636)Coloplast A/S1988-07-13
EMERGENCY-CLEAN UP(TM) ECP (K880306)Cdc Products Corp.1988-05-20
COMBINATION NITE DRAINAGE UNIT (K872294)Arnold Technologies1987-12-29
'CATCH-IT' OR FECAL CONTAINMENT DEVICE (K873929)Midwest Medical Co.1987-12-03
ODOR-SAFE(TM)(LIQUID) ODOR-SAFE(TM) POWDER (K871526)Cox Family Laboratories, Inc.1987-10-13
OSTO-PURE (K871738)Clearchem Corp.1987-08-12
PALEX (R) OSTOMY (K871628)Industrias Palex C/O Dma Med-Chem Corp.1987-07-08

Recalls involving this device

No recalls on record reference this clearance.