FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

METATECH MICROCLIP APPLICATOR

K Number: K882367 · Decision Aug 25, 1988
Classifications
1
FEI Numbers
313
Registration Numbers
313
Same Product Code
70
Applicant Total
13
Review Days
78

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Basic Information

Device Name
METATECH MICROCLIP APPLICATOR
K Number
K882367
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
870.4500
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Metatech Corp.
Date Received
June 8, 1988
Decision Date
August 25, 1988
Product Code
DWS
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

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

Product Code Device Name
DWS Instruments, Surgical, Cardiovascular

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Other Clearances by Metatech Corp.

K Number Device Name
K924314 MOBILE STANDING FRAME
K915370 COPPER VAPOR LASER SYSTEM
K903883 VASCULASE(R) COPPER VAPOR LASER SYST, PIGMENT LES
K890865 HEXASCAN SCANNER HANDPIECE
K883541 METALASER VASCULASE
K883881 MODIFIED MODEL 2001 FIBER OPTICS CATHETER
K883518 EVENT MARKER & A SECOND PRESSURE TREND OUTPUT
K882552 METATECH ROBINSON BOLT ACCESSORY
K882286 EXPANSION COUPLER & MANUAL DRILL AS ACCESSORY SET
K881447 METATECH METAL MICROCLIP
Search all 13 clearances from Metatech Corp. →