FDA 510(k)

ANAEROBE PEA PLATE

K-Number: K822527 · 1982-09-30

Decision Date1982-09-30

Product CodeJSJ

Advisory CommitteeMI

DecisionSubstantially Equivalent

Device Summary

ANAEROBE PEA PLATE 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 1982-09-30 under 510(k) number K822527. 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 ANAEROBE PEA PLATE?

ANAEROBE PEA PLATE is a medical device that received FDA 510(k) clearance on 1982-09-30. The listed applicant is Granite Diagnostics, Inc.. The 510(k) number is K822527.

When did ANAEROBE PEA PLATE receive FDA 510(k) clearance?

ANAEROBE PEA PLATE received FDA 510(k) clearance on 1982-09-30, under 510(k) number K822527.

Who is the listed applicant for ANAEROBE PEA PLATE?

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 ANAEROBE PEA PLATE?

The FDA product code for ANAEROBE PEA PLATE is 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.