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FDA 510(k)

DUAL PEDESTAL TABLE

K-Number: K811969 · 1981-08-13

ApplicantPhilips Medical Systems (Cleveland), Inc.
Decision Date1981-08-13
Product CodeKXJ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DUAL PEDESTAL TABLE 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 1981-08-13 under 510(k) number K811969. The device is classified under product code KXJ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DUAL PEDESTAL TABLE?

DUAL PEDESTAL TABLE is a medical device that received FDA 510(k) clearance on 1981-08-13. The listed applicant is Philips Medical Systems (Cleveland), Inc.. The 510(k) number is K811969.

When did DUAL PEDESTAL TABLE receive FDA 510(k) clearance?

DUAL PEDESTAL TABLE received FDA 510(k) clearance on 1981-08-13, under 510(k) number K811969.

Who is the listed applicant for DUAL PEDESTAL TABLE?

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 DUAL PEDESTAL TABLE?

The FDA product code for DUAL PEDESTAL TABLE is KXJ.

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Related Devices (Code: KXJ)

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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