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FDA 510(k)

SCHAEDLER AGARS

K-Number: K823248 · 1982-12-03

ApplicantGranite Diagnostics, Inc.
Decision Date1982-12-03
Product CodeJSJ
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

SCHAEDLER AGARS is the device name listed in this FDA 510(k) record. The listed applicant is Granite Diagnostics, Inc.. It received FDA 510(k) clearance on 1982-12-03 under 510(k) number K823248. The device is classified under product code JSJ. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SCHAEDLER AGARS?

SCHAEDLER AGARS is a medical device that received FDA 510(k) clearance on 1982-12-03. The listed applicant is Granite Diagnostics, Inc.. The 510(k) number is K823248.

When did SCHAEDLER AGARS receive FDA 510(k) clearance?

SCHAEDLER AGARS received FDA 510(k) clearance on 1982-12-03, under 510(k) number K823248.

Who is the listed applicant for SCHAEDLER AGARS?

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

What is the FDA product code for SCHAEDLER AGARS?

The FDA product code for SCHAEDLER AGARS is JSJ.

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Other records listing Granite Diagnostics, Inc. as applicant

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Related Devices (Code: JSJ)

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Official Source

View on FDA Database →

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

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