Atlas FDA

RX IV PENTRON IV

FDA 510(k) clearance K833285 · decided 1983-12-22

Clearance details

K-number
K833285
Device name
RX IV PENTRON IV
Applicant
Genesis Industries, Inc.
Decision
Substantially Equivalent
Date received
1983-09-22
Decision date
1983-12-22
Days to decision
91 days
Clearance type
Traditional
Product code
EIS
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
ATD AUTOMATIC BRIDGE REMOVER (K992649)J. Morita USA, Inc.1999-10-29
EASY PNEUMATIC CROWN AND BRIDGE REMOVER (K951299)Dentco, Inc.1995-08-29
STAINLESS STEEL DEN. CROWN REMOVER & AMA./COMP.CAR (K863500)Pacific Union Dental, Inc.1986-09-22
HAZELTON TEMPORARY CROWN AND BRIDGE REMOVER (K854795)Fran Hazelton Co.1986-03-04
H-TYPE BRIDGE REMOVER (K842026)Higa Manufacturing , Ltd.1984-07-11
SATIN CAST ECONOCAST (K833287)Genesis Industries, Inc.1984-01-03
C & B 40 PENTRO C & B40 (K833290)Genesis Industries, Inc.1984-01-03
C & B 45 (K833278)Genesis Industries, Inc.1983-12-29
GOLD-PALLADIUM-SILVER BASED CAST/ALLOY (K833736)Jeneric Ind.1983-12-29
C & B 61 PENTRON C & B61 (K833289)Genesis Industries, Inc.1983-12-29
SUPRA AP CHOICE 83 (K833280)Genesis Industries, Inc.1983-12-26
C & B57 PENTRON C & B57 (K833288)Genesis Industries, Inc.1983-12-20

Recalls involving this device

No recalls on record reference this clearance.