Atlas FDA

INJECT-R FILL

FDA 510(k) clearance K931742 · decided 1993-05-27

Clearance details

K-number
K931742
Device name
INJECT-R FILL
Applicant
Union Broach, Div. Moyco Industries, Inc.
Decision
Substantially Equivalent
Date received
1993-04-07
Decision date
1993-05-27
Days to decision
50 days
Clearance type
Traditional
Product code
EKM
Device class
1
Regulation number
872.3850
Medical specialty
Dental
Advisory committee
Dental
Location
Emigsville, PA, 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
EI DOWNPAK BARRIER SLEEVES (K073369)Hu-Friedy Mfg. Co., Inc.2008-02-27
DOWN PAK (K070246)Endo Twinn B.V.2007-02-16
TGP (GUTTA PERCHA CONTAINING TETRACYCLINE OR DOXYCYCLINE) (K051573)Dr. Howard Martin, P.A.2006-06-26
ENDO TWINN (K042870)Endo Twinn B.V.2005-01-11
FIBERFILL SGP (K023819)Pentron Clinical Technologies2003-03-26
ANTIBACTERIAL GUTTA PERCHA (K971641)Dr. Howard Martin, P.A.1997-07-21
THERMAPREP PLUS OVEN (K970134)Tulsa Dental Products, Ltd.1997-03-21
MICRODOSE RC-EZ (K924825)Unicep1993-03-05
TOUCH 'N HEAT MODEL 5002, MODIFICATION (K915243)Analytic Technology1992-01-21
THERMAPREP (K910224)Tulsa Dental Products, Ltd.1991-03-29
THERMAFIL ENDODONTIC OBTURATOR (K900986)Tulsa Dental Products, Ltd.1990-11-13
ENDO-PREP (K896663)Pulpdent Corp.1990-02-14

Recalls involving this device

No recalls on record reference this clearance.