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FDA 510(k)

AIA-PACK HCG CALIBRATION VERIFICATION TEST SET

K-Number: K924862 · 1992-12-28

ApplicantTosoh Medics, Inc.
Decision Date1992-12-28
Product CodeJJX
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

AIA-PACK HCG CALIBRATION VERIFICATION TEST SET is the device name listed in this FDA 510(k) record. The listed applicant is Tosoh Medics, Inc.. It received FDA 510(k) clearance on 1992-12-28 under 510(k) number K924862. The device is classified under product code JJX. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AIA-PACK HCG CALIBRATION VERIFICATION TEST SET?

AIA-PACK HCG CALIBRATION VERIFICATION TEST SET is a medical device that received FDA 510(k) clearance on 1992-12-28. The listed applicant is Tosoh Medics, Inc.. The 510(k) number is K924862.

When did AIA-PACK HCG CALIBRATION VERIFICATION TEST SET receive FDA 510(k) clearance?

AIA-PACK HCG CALIBRATION VERIFICATION TEST SET received FDA 510(k) clearance on 1992-12-28, under 510(k) number K924862.

Who is the listed applicant for AIA-PACK HCG CALIBRATION VERIFICATION TEST SET?

The FDA 510(k) record lists Tosoh Medics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AIA-PACK HCG CALIBRATION VERIFICATION TEST SET?

The FDA product code for AIA-PACK HCG CALIBRATION VERIFICATION TEST SET is JJX.

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Other records listing Tosoh Medics, Inc. as applicant

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Related Devices (Code: JJX)

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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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