HELIODENT DS— 510(k) K960819

Substantially Equivalent

Pelton & Crane Co.

FDA 510(k) clearance K960819 for HELIODENT DS, Substantially Equivalent on 1996-03-29. Applicant: Pelton & Crane Co.. Device class: 2.

Clearance details

Applicant: Pelton & Crane Co.
Product code: Code EAP
Device class: Class 2
Regulation: 21 CFR 872.1810
Advisory panel: Dental
Date received: 1996-02-29
Decision date: 1996-03-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Charlotte, NC, US

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More clearances from Pelton & Crane Co.

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K945117 — DELTA1997-02-28
K962071 — SPIRIT S1/S21996-08-06
K950299 — CEREC 21995-05-23

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