RX NYSP PENTRON 60— 510(k) K833282

Substantially Equivalent

Genesis Industries, Inc.

FDA 510(k) clearance K833282 for RX NYSP PENTRON 60, Substantially Equivalent on 1983-11-28. Applicant: Genesis Industries, Inc.. Device class: 1.

Clearance details

Applicant: Genesis Industries, Inc.
Product code: Code EIS
Device class: Class 1
Regulation: 21 CFR 872.4565
Advisory panel: Dental
Date received: 1983-09-22
Decision date: 1983-11-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code EIS

K992649 — ATD AUTOMATIC BRIDGE REMOVER1999-10-29
K951299 — EASY PNEUMATIC CROWN AND BRIDGE REMOVER1995-08-29
K863500 — STAINLESS STEEL DEN. CROWN REMOVER & AMA./COMP.CAR1986-09-22
K854795 — HAZELTON TEMPORARY CROWN AND BRIDGE REMOVER1986-03-04
K842026 — H-TYPE BRIDGE REMOVER1984-07-11

More clearances from Genesis Industries, Inc.

K994361 — ESP FOUR WELL TISSUE CULTURE PLATE, ESP SIX WELL TISSUE CULTURE PLATE, ESP MICRO SIX WELL TISSUE CULTURE PLATE, ESP WELL2000-02-18
K962828 — EVERT-IT1997-02-10
K880377 — NOVO VIVO MODEL #17140 AND #171351988-04-04
K880376 — NOVO VIVO SUCTION CATHETER VESSEL W/MUCOSE TRAP1988-02-16
K833287 — SATIN CAST ECONOCAST1984-01-03

Data sourced from openFDA. This site is unofficial and independent of the FDA.