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FDA 510(k)

FORAMATRON V, MODEL D680

K-Number: K002195 · 2000-08-30

ApplicantParkell, Inc.
Decision Date2000-08-30
Product CodeLQY
DecisionSubstantially Equivalent

Device Summary

FORAMATRON V, MODEL D680 is the device name listed in this FDA 510(k) record. The listed applicant is Parkell, Inc.. It received FDA 510(k) clearance on 2000-08-30 under 510(k) number K002195. The device is classified under product code LQY. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FORAMATRON V, MODEL D680?

FORAMATRON V, MODEL D680 is a medical device that received FDA 510(k) clearance on 2000-08-30. The listed applicant is Parkell, Inc.. The 510(k) number is K002195.

When did FORAMATRON V, MODEL D680 receive FDA 510(k) clearance?

FORAMATRON V, MODEL D680 received FDA 510(k) clearance on 2000-08-30, under 510(k) number K002195.

Who is the listed applicant for FORAMATRON V, MODEL D680?

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 V, MODEL D680?

The FDA product code for FORAMATRON V, MODEL D680 is 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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