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FDA 510(k)

ACQPLAN

K-Number: K974770 · 1998-09-02

ApplicantPhilips Medical Systems (Cleveland), Inc.
Decision Date1998-09-02
Product CodeMUJ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ACQPLAN is the device name listed in this FDA 510(k) record. The listed applicant is Philips Medical Systems (Cleveland), Inc.. It received FDA 510(k) clearance on 1998-09-02 under 510(k) number K974770. The device is classified under product code MUJ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACQPLAN?

ACQPLAN is a medical device that received FDA 510(k) clearance on 1998-09-02. The listed applicant is Philips Medical Systems (Cleveland), Inc.. The 510(k) number is K974770.

When did ACQPLAN receive FDA 510(k) clearance?

ACQPLAN received FDA 510(k) clearance on 1998-09-02, under 510(k) number K974770.

Who is the listed applicant for ACQPLAN?

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

What is the FDA product code for ACQPLAN?

The FDA product code for ACQPLAN is MUJ.

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Other records listing Philips Medical Systems (Cleveland), Inc. as applicant

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Related Devices (Code: MUJ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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