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FDA 510(k)

FORAMATRON IV

K-Number: K950857 · 1995-04-20

ApplicantParkell, Inc.
Decision Date1995-04-20
Product CodeLQY
DecisionSubstantially Equivalent

Device Summary

FORAMATRON IV is the device name listed in this FDA 510(k) record. The listed applicant is Parkell, Inc.. It received FDA 510(k) clearance on 1995-04-20 under 510(k) number K950857. The device is classified under product code LQY. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FORAMATRON IV?

FORAMATRON IV is a medical device that received FDA 510(k) clearance on 1995-04-20. The listed applicant is Parkell, Inc.. The 510(k) number is K950857.

When did FORAMATRON IV receive FDA 510(k) clearance?

FORAMATRON IV received FDA 510(k) clearance on 1995-04-20, under 510(k) number K950857.

Who is the listed applicant for FORAMATRON IV?

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

What is the FDA product code for FORAMATRON IV?

The FDA product code for FORAMATRON IV is LQY.

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Other records listing Parkell, Inc. as applicant

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Related Devices (Code: LQY)

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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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