FDA 510(k)

N-A-G TEST KIT

K-Number: K893582 · 1990-10-01

Decision Date1990-10-01

Product CodeCGX

Advisory CommitteeCH

DecisionSubstantially Equivalent

Device Summary

N-A-G TEST KIT is the device name listed in this FDA 510(k) record. The listed applicant is Ppr Diagnostics , Ltd.. It received FDA 510(k) clearance on 1990-10-01 under 510(k) number K893582. The device is classified under product code CGX. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the N-A-G TEST KIT?

N-A-G TEST KIT is a medical device that received FDA 510(k) clearance on 1990-10-01. The listed applicant is Ppr Diagnostics , Ltd.. The 510(k) number is K893582.

When did N-A-G TEST KIT receive FDA 510(k) clearance?

N-A-G TEST KIT received FDA 510(k) clearance on 1990-10-01, under 510(k) number K893582.

Who is the listed applicant for N-A-G TEST KIT?

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

What is the FDA product code for N-A-G TEST KIT?

The FDA product code for N-A-G TEST KIT is CGX.

Related Devices (Code: CGX)

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.

K252206Nova Allegro UACR Assay, Nova Allegro AnalyzerNova Biomedical Corporation K251058Tru Kidney Health Test Panel; Tru AnalyzerTruvian Health K242685Atellica® CH Creatinine_3 (Crea3)Siemens Healthcare Diagnostics, Inc.K221813Nova Allegro UACR Assay, Nova Allegro AnalyzerNova Biomedical Corporation K210452Creatinine2Abbott Ireland Diagnostics Division K161494Atellica CH Creatinine_2 (Crea_2), Atellica CH Chemistry Calibrator (CHEM CAL)Siemens Healthcare Diagnostics, Inc.

Official Source

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