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FDA 510(k)

PIASTRINIT

K-Number: K863114 · 1986-11-06

ApplicantJ. D. Assoc.
Decision Date1986-11-06
Product CodeGGK
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

PIASTRINIT is the device name listed in this FDA 510(k) record. The listed applicant is J. D. Assoc.. It received FDA 510(k) clearance on 1986-11-06 under 510(k) number K863114. The device is classified under product code GGK. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PIASTRINIT?

PIASTRINIT is a medical device that received FDA 510(k) clearance on 1986-11-06. The listed applicant is J. D. Assoc.. The 510(k) number is K863114.

When did PIASTRINIT receive FDA 510(k) clearance?

PIASTRINIT received FDA 510(k) clearance on 1986-11-06, under 510(k) number K863114.

Who is the listed applicant for PIASTRINIT?

The FDA 510(k) record lists J. D. Assoc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PIASTRINIT?

The FDA product code for PIASTRINIT is GGK.

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Other records listing J. D. Assoc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K863054AST S.C.E. (GOT)K863103PEG 6,000K863069MAGNESIOMETERK863079CREATINKINETICK863112PROTEINMETERK863053ALT S.C.E. (GPT)

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Related Devices (Code: GGK)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K883836COULTER CLONE QUICK STAIN WHOLE BLOOD LYSE-IICoulter ImmunologyK883991KVM HEMOGLOBIN LYSING REAGENTKvm Technologies, Inc.K874054FISHER DIAGNOSTICS HEMATALL III LAS REAGENTFisher Scientific Co., LLCK873348CELL-DYN DIFF SCREEN, AUTO. & SEMI AUTO. LYTIC AG.Abbott DiagnosticsK863503HEMOLYSEReagent Laboratory, Inc.K850097LASER-LYSEHematology Marketing Assoc.

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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