Atlas FDA

CENTRIX MKIV ENDODONTIC DELIVERY

FDA 510(k) clearance K792461 · decided 1979-12-19

Clearance details

K-number
K792461
Device name
CENTRIX MKIV ENDODONTIC DELIVERY
Applicant
Centrix, Inc.
Decision
Substantially Equivalent
Date received
1979-12-03
Decision date
1979-12-19
Days to decision
16 days
Clearance type
Traditional
Product code
EIC
Device class
1
Regulation number
872.4565
Medical specialty
Dental
Advisory committee
Dental
Location
Mchenry, IL, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
RCT GEL ROOT CANAL THERAPY GEL (K972234)Dentsply Intl.1997-06-30
MAX-I-PROBE PERIDONTAL/ENDODONTIC PROBE(TM) (MODI) (K864307)Smith & Nephew, Inc.1986-11-18
HYDRON ROOT CANAL FILLING & MARK IV STARTER KIT (K861846)Solar Dental Co., Inc.1986-06-26
MAX-I-PROBE HANDPIECE (K851944)Solo Pak Laboratories1985-07-01
MAX-I-PROBE PERIODONTAL ENDODONTIC PROB (K840237)Smith & Nephew, Mpl Division1984-04-05
R & S SERIES FITTING TOOLS (K811889)Suncoast Dental Corp.1981-07-24
WATER PISTOL (K811594)Aus-Tex Dental Mfg. & Design1981-07-15
ROOT CANAL FILLING APPLICATOR NEEDLES (K801484)National Patent Development Corp.1980-07-21
MARK IV SYRINGE (K801483)National Patent Development Corp.1980-07-21
EPIC CANNULA (K792578)Dental Development Services, Inc.1980-01-04
ENDOVAGE SYRINGE (K792577)Dental Development Services, Inc.1980-01-04
GUTTA GUN (K771406)Aus-Tex Dental Mfg. & Design1977-08-26

Recalls involving this device

No recalls on record reference this clearance.