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

BOARD, DISPOSABLE CONTROL COUNT

K Number: K781791 · Decision Nov 8, 1978
Classifications
1
FEI Numbers
92
Registration Numbers
92
Same Product Code
112
Applicant Total
38
Review Days
19

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Basic Information

Device Name
BOARD, DISPOSABLE CONTROL COUNT
K Number
K781791
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5570
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Dexide, Inc.
Date Received
October 20, 1978
Decision Date
November 8, 1978
Product Code
MMK
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
MMK Container, Sharps

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Other Clearances by Dexide, Inc.

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K981940 MULTAPUMP DISPOSABLE PUMP HEAD AND ACCESSORIES
K981941 MULTAPORT CANNULA REDUCER AND ACCESSORIES
K953611 DEXIDE ENDO-LUBE KIT
K944509 DEXIDE INSUFFLATION TUBING WITH FILTER
K924117 DEXIDE LAPAROSCOPIC KITS
K923845 DEXIDE LAPAROSCOPIC ACCESSORIES
K921709 ENDOBAG, MODIFICATION
K913762 MONOSCOPY(TM) BRAND, ENDOBAG
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