Atlas FDA

KARAYA GUM POWDER, OSTOMY

FDA 510(k) clearance K770408 · decided 1977-03-15

Clearance details

K-number
K770408
Device name
KARAYA GUM POWDER, OSTOMY
Applicant
Howmedica Corp.
Decision
Substantially Equivalent
Date received
1977-03-04
Decision date
1977-03-15
Days to decision
11 days
Clearance type
Traditional
Product code
EZK
Device class
2
Regulation number
876.5980
Medical specialty
Gastroenterology, Urology
Advisory committee
Gastroenterology, Urology
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
E-Z-EM ENTEROCLYSIS CATHETER SET (K911349)E-Z-Em, Inc.1992-11-16
URINE METER FOLEY TRAY WITH TEMPERATURE SENSOR (K903816)Respiratory Support Products, Inc.1990-10-31

Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
SURGICAL SIMPLEX P BONE CEMENT (N17004/S013)Howmedica Corp.2000-12-15
SURGICAL SIMPLEX P RADIOPAQUE BONE CEMENT (N17004/S012)Howmedica Corp.2000-06-20
SURGICAL SIMPLEX(R) P RADIOPAQUE BONE CEMENT (N17004/S011)Howmedica Corp.1998-03-18
SURGICAL SIMPLEX(R) P RADIOPAQUE BONE CEMENT (N17004/S010)Howmedica Corp.1997-11-13
SURGICAL SIMPLEX(R) P RADIOPAQUE BONE CEMENT (N17004/S009)Howmedica Corp.1997-08-08
SURGICAL SIMPLEX(R) P RADIOPAQUE BONE CEMENT (N17004/S008)Howmedica Corp.1996-12-18
SURGICAL SIMPLEX(R) P RADIOPAQUE BONE CEMENT (N17004/S005)Howmedica Corp.1995-11-21
SURGICAL SIMPLEX(R) P RADIOPAQUE BONE CEMENT (N17004/S006)Howmedica Corp.1995-02-24