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

CARAPACE EPIDURAL BLOCK & SPINAL MYELOGRAM TRAYS

K Number: K931670 · Decision Jan 25, 1994
Classifications
1
FEI Numbers
81
Registration Numbers
81
Same Product Code
154
Applicant Total
22
Review Days
294

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Basic Information

Device Name
CARAPACE EPIDURAL BLOCK & SPINAL MYELOGRAM TRAYS
K Number
K931670
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5140
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Carapace, Inc.
Date Received
April 6, 1993
Decision Date
January 25, 1994
Product Code
CAZ
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

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

Product Code Device Name
CAZ Anesthesia Conduction Kit

Similar 510(k) Clearances

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

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Other Clearances by Carapace, Inc.

K Number Device Name
K931722 CARAPACE LABOR AND DELIVERY SETS
K931822 CARAPACE PELVIC EXAM TRAYS
K931729 I.V. START KIT
K931820 CARAPACE STILLWATER BOWL SET
K931669 CARAPACE DEBRIDEMENT KITS
K931760 CARAPACE PACKING GAUZE TRAYS
K932653 SWISSTEK 2000(TM) CAST REMOVAL SYSTEM
K931758 CARAPACE WOUND DRESSING KITS & LACERATION TRAYS
K931819 CARAPACE SUTURE REMOVAL TRAYS
K931759 CARAPACE STERILE GAUZE TRAYS
Search all 22 clearances from Carapace, Inc. →