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FDA 510(k)

INCLINOMETER, VERMONT

K-Number: K781982 · 1978-12-04

ApplicantAssociates IN Radiology, Inc.
Decision Date1978-12-04
Product CodeIZL
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

INCLINOMETER, VERMONT is the device name listed in this FDA 510(k) record. The listed applicant is Associates IN Radiology, Inc.. It received FDA 510(k) clearance on 1978-12-04 under 510(k) number K781982. The device is classified under product code IZL. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INCLINOMETER, VERMONT?

INCLINOMETER, VERMONT is a medical device that received FDA 510(k) clearance on 1978-12-04. The listed applicant is Associates IN Radiology, Inc.. The 510(k) number is K781982.

When did INCLINOMETER, VERMONT receive FDA 510(k) clearance?

INCLINOMETER, VERMONT received FDA 510(k) clearance on 1978-12-04, under 510(k) number K781982.

Who is the listed applicant for INCLINOMETER, VERMONT?

The FDA 510(k) record lists Associates IN Radiology, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INCLINOMETER, VERMONT?

The FDA product code for INCLINOMETER, VERMONT is IZL.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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