FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

BILIARY STONE DISLODGER

K Number: K925559 · Decision Dec 17, 1992
Classifications
1
FEI Numbers
41
Registration Numbers
41
Same Product Code
37
Applicant Total
23
Review Days
44

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Basic Information

Device Name
BILIARY STONE DISLODGER
K Number
K925559
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5010
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Annex Medical, Inc.
Date Received
November 3, 1992
Decision Date
December 17, 1992
Product Code
LQR
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LQR Dislodger, Stone, Biliary

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (LQR), ordered by most recent decision date.

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Other Clearances by Annex Medical, Inc.

K Number Device Name
K954377 FORCEPS, GRASPING, FLEXIBLE ENDOSCOPIC
K952863 FORCEPS, BIOPSY, NON-ELECTRIC
K951532 METAL URETERAL BASKET STONE DISLODGER
K951761 METEL URETERAL BASKET STONE DISLODGER
K934636 ANNEX MEDICAL FLAT WIRE STONE EXTRACTOR
K934675 METAL URETERAL BASKET STONE DISLODGER
K934598 GRASPING FORCEPS OR RETRIEVAL FORCEPS
K925267 GRASPING FORCEPS OR RETRIEVAL FORCEPS
K921401 BIOPSY FORCEPS
K924027 DISLODGER, STONE, BASKET, URETERAL, METAL
Search all 23 clearances from Annex Medical, Inc. →