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FDA 510(k)

POWER EXAMINATION TABLE

K-Number: K882010 · 1988-07-13

ApplicantEnochs Mfg., Inc.
Decision Date1988-07-13
Product CodeLGX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

POWER EXAMINATION TABLE is the device name listed in this FDA 510(k) record. The listed applicant is Enochs Mfg., Inc.. It received FDA 510(k) clearance on 1988-07-13 under 510(k) number K882010. The device is classified under product code LGX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POWER EXAMINATION TABLE?

POWER EXAMINATION TABLE is a medical device that received FDA 510(k) clearance on 1988-07-13. The listed applicant is Enochs Mfg., Inc.. The 510(k) number is K882010.

When did POWER EXAMINATION TABLE receive FDA 510(k) clearance?

POWER EXAMINATION TABLE received FDA 510(k) clearance on 1988-07-13, under 510(k) number K882010.

Who is the listed applicant for POWER EXAMINATION TABLE?

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

What is the FDA product code for POWER EXAMINATION TABLE?

The FDA product code for POWER EXAMINATION TABLE is LGX.

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Related Devices (Code: LGX)

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.

K945163ECHOCARDIOGRAPHYTri W-G, Inc.K894144POWER EXAMINATION TABLE MODEL # 405Midmark Corp.K894134POWER EXAMINATION TABLE MODEL # 411Midmark Corp.K883680MEDALIST EXAMINATION TABLEHamilton Industries, Inc.K864072ADEC 1005-C CHAIRCherne Industries, Inc.K860519RELIANCE MODEL 200 PODIATRY CHAIRF. & F. Koenigkramer

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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