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FDA 510(k)

RELLPLATE C KIT, RELLPLATE C BULK PLATES

K-Number: K884940 · 1989-03-13

ApplicantAmerican Diagnostic Corp.
Decision Date1989-03-13
Product CodeGGP
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

RELLPLATE C KIT, RELLPLATE C BULK PLATES is the device name listed in this FDA 510(k) record. The listed applicant is American Diagnostic Corp.. It received FDA 510(k) clearance on 1989-03-13 under 510(k) number K884940. The device is classified under product code GGP. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RELLPLATE C KIT, RELLPLATE C BULK PLATES?

RELLPLATE C KIT, RELLPLATE C BULK PLATES is a medical device that received FDA 510(k) clearance on 1989-03-13. The listed applicant is American Diagnostic Corp.. The 510(k) number is K884940.

When did RELLPLATE C KIT, RELLPLATE C BULK PLATES receive FDA 510(k) clearance?

RELLPLATE C KIT, RELLPLATE C BULK PLATES received FDA 510(k) clearance on 1989-03-13, under 510(k) number K884940.

Who is the listed applicant for RELLPLATE C KIT, RELLPLATE C BULK PLATES?

The FDA 510(k) record lists American Diagnostic Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RELLPLATE C KIT, RELLPLATE C BULK PLATES?

The FDA product code for RELLPLATE C KIT, RELLPLATE C BULK PLATES is GGP.

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Other records listing American Diagnostic Corp. as applicant

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Related Devices (Code: GGP)

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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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