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FDA 510(k)

HAEMOPHILUS ID PLATE

K-Number: K822377 · 1982-08-25

ApplicantGranite Diagnostics, Inc.
Decision Date1982-08-25
Product CodeJSH
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

HAEMOPHILUS ID 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 1982-08-25 under 510(k) number K822377. The device is classified under product code JSH. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HAEMOPHILUS ID PLATE?

HAEMOPHILUS ID PLATE is a medical device that received FDA 510(k) clearance on 1982-08-25. The listed applicant is Granite Diagnostics, Inc.. The 510(k) number is K822377.

When did HAEMOPHILUS ID PLATE receive FDA 510(k) clearance?

HAEMOPHILUS ID PLATE received FDA 510(k) clearance on 1982-08-25, under 510(k) number K822377.

Who is the listed applicant for HAEMOPHILUS ID 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 HAEMOPHILUS ID PLATE?

The FDA product code for HAEMOPHILUS ID PLATE is JSH.

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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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