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FDA 510(k)

MODEL 2600 PROCART

K-Number: K941476 · 1994-09-02

ApplicantCompressor Technologies, Ltd.
Decision Date1994-09-02
Product CodeEIA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MODEL 2600 PROCART is the device name listed in this FDA 510(k) record. The listed applicant is Compressor Technologies, Ltd.. It received FDA 510(k) clearance on 1994-09-02 under 510(k) number K941476. The device is classified under product code EIA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 2600 PROCART?

MODEL 2600 PROCART is a medical device that received FDA 510(k) clearance on 1994-09-02. The listed applicant is Compressor Technologies, Ltd.. The 510(k) number is K941476.

When did MODEL 2600 PROCART receive FDA 510(k) clearance?

MODEL 2600 PROCART received FDA 510(k) clearance on 1994-09-02, under 510(k) number K941476.

Who is the listed applicant for MODEL 2600 PROCART?

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

What is the FDA product code for MODEL 2600 PROCART?

The FDA product code for MODEL 2600 PROCART is EIA.

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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.

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