ABIOMED PERIOTEMP(TM) PROBE— 510(k) K885075

Substantially Equivalent

Abiomed, Inc.

FDA 510(k) clearance K885075 for ABIOMED PERIOTEMP(TM) PROBE, Substantially Equivalent on 1989-02-13. Applicant: Abiomed, Inc.. Device class: 1.

Clearance details

Applicant: Abiomed, Inc.
Product code: Code EIL
Device class: Class 1
Regulation: 21 CFR 872.4565
Advisory panel: Dental
Date received: 1988-12-08
Decision date: 1989-02-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Danvers, MA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code EIL

K911643 — ABIODENT PERIOTEMP(R) SYSTEM1991-07-09
K890493 — FLORIDA PROBE PERIODONTAL PROBE1989-03-13
K884813 — MODEL 200A ELECTRONIC FORCE-SENSING PROBE1989-01-05
K880209 — PERIODONTAL PROBE - AUTOPROBE1988-04-27
K872098 — CREMEEN ALVEOLAR BONE CALIPER1987-07-31

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