ZEPPELIN INSTRUMENTS— 510(k) K902850

Substantially Equivalent

Ruggles Corp.

FDA 510(k) clearance K902850 for ZEPPELIN INSTRUMENTS, Substantially Equivalent on 1990-07-18. Applicant: Ruggles Corp.. Device class: 1.

Clearance details

Applicant: Ruggles Corp.
Product code: Code HAO
Device class: Class 1
Regulation: 21 CFR 882.4535
Advisory panel: Neurology
Date received: 1990-06-29
Decision date: 1990-07-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: No. Quincy, MA, US

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More clearances from Ruggles Corp.

K903485 — TITANIUM MESH1991-02-21
K902818 — MULTIPLE NONPOWERED NEUROSURGICAL INSTRUMENT1990-09-20
K902819 — LAMINECTOMY ROGEUR1990-08-09
K893415 — TRANS-ORAL DEPTH GAUGE1989-06-07

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