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FDA 510(k)

AIA-PACK PA CALIBRATION VERIFICATION/LINEARITY TES

K-Number: K932178 · 1993-09-21

ApplicantTosoh Medics, Inc.
Decision Date1993-09-21
Product CodeJJX
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

AIA-PACK PA CALIBRATION VERIFICATION/LINEARITY TES 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 1993-09-21 under 510(k) number K932178. 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 PA CALIBRATION VERIFICATION/LINEARITY TES?

AIA-PACK PA CALIBRATION VERIFICATION/LINEARITY TES is a medical device that received FDA 510(k) clearance on 1993-09-21. The listed applicant is Tosoh Medics, Inc.. The 510(k) number is K932178.

When did AIA-PACK PA CALIBRATION VERIFICATION/LINEARITY TES receive FDA 510(k) clearance?

AIA-PACK PA CALIBRATION VERIFICATION/LINEARITY TES received FDA 510(k) clearance on 1993-09-21, under 510(k) number K932178.

Who is the listed applicant for AIA-PACK PA CALIBRATION VERIFICATION/LINEARITY TES?

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 PA CALIBRATION VERIFICATION/LINEARITY TES?

The FDA product code for AIA-PACK PA CALIBRATION VERIFICATION/LINEARITY TES 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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