FDA 510(k) FDA class 1 Unknown 🇺🇸 United States

DEXIDE LAPAROSCOPIC KITS

K Number: K924117 · Decision Mar 23, 1993
Classifications
1
FEI Numbers
329
Registration Numbers
330
Same Product Code
61
Applicant Total
38
Review Days
221

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Basic Information

Device Name
DEXIDE LAPAROSCOPIC KITS
K Number
K924117
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Unknown
Statement or Summary
Statement
Applicant
Dexide, Inc.
Date Received
August 14, 1992
Decision Date
March 23, 1993
Product Code
KDD
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
KDD Kit, Surgical Instrument, Disposable

Similar 510(k) Clearances

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Other Clearances by Dexide, Inc.

K Number Device Name
K991814 MULTACHOICE INSTRUMENTS
K990379 MODIFICATION TO MULTAPORT CANNULA, REDUCER AND ACCESSORIES
K981940 MULTAPUMP DISPOSABLE PUMP HEAD AND ACCESSORIES
K981941 MULTAPORT CANNULA REDUCER AND ACCESSORIES
K953611 DEXIDE ENDO-LUBE KIT
K944509 DEXIDE INSUFFLATION TUBING WITH FILTER
K923845 DEXIDE LAPAROSCOPIC ACCESSORIES
K921709 ENDOBAG, MODIFICATION
K913762 MONOSCOPY(TM) BRAND, ENDOBAG
K912637 LAPAROSCOPIC ELECTROSURGICAL CANNULA W/RETRACTABLE
Search all 38 clearances from Dexide, Inc. →