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

DENTAL SURGICAL WRAP #3007 A,B,C

K Number: K891214 · Decision Apr 14, 1989
Classifications
1
FEI Numbers
266
Registration Numbers
266
Same Product Code
279
Applicant Total
7
Review Days
38

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Basic Information

Device Name
DENTAL SURGICAL WRAP #3007 A,B,C
K Number
K891214
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.6850
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Pro-Safe Professional Linens, Inc.
Date Received
March 7, 1989
Decision Date
April 14, 1989
Product Code
KCT
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
KCT Sterilization Wrap Containers, Trays, Cassettes & Other Accessories

Similar 510(k) Clearances

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

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Other Clearances by Pro-Safe Professional Linens, Inc.

K Number Device Name
K891210 POCKETED WRAPS #3009 A,B,C
K891216 DENTAL EQUIPMENT PROTECTION DEVICES
K891211 SURGICAL GOWN #2001
K891212 APRONS, SCRUBS SLACKS & TOPS, PATIENT DRAPE
K891213 SURGICAL INSTRUMENT POUCH #M102
K891215 FAST WRAP #M 101