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FDA 510(k)

DELUXE ELECTRIC COMBINATION TILT TABLE

K-Number: K924019 · 1992-11-06

ApplicantMidland Mfg. Co.
Decision Date1992-11-06
Product CodeINQ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

DELUXE ELECTRIC COMBINATION TILT TABLE is the device name listed in this FDA 510(k) record. The listed applicant is Midland Mfg. Co.. It received FDA 510(k) clearance on 1992-11-06 under 510(k) number K924019. The device is classified under product code INQ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DELUXE ELECTRIC COMBINATION TILT TABLE?

DELUXE ELECTRIC COMBINATION TILT TABLE is a medical device that received FDA 510(k) clearance on 1992-11-06. The listed applicant is Midland Mfg. Co.. The 510(k) number is K924019.

When did DELUXE ELECTRIC COMBINATION TILT TABLE receive FDA 510(k) clearance?

DELUXE ELECTRIC COMBINATION TILT TABLE received FDA 510(k) clearance on 1992-11-06, under 510(k) number K924019.

Who is the listed applicant for DELUXE ELECTRIC COMBINATION TILT TABLE?

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

What is the FDA product code for DELUXE ELECTRIC COMBINATION TILT TABLE?

The FDA product code for DELUXE ELECTRIC COMBINATION TILT TABLE is INQ.

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Other records listing Midland Mfg. Co. as applicant

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.

K933311MOTORIZED ELECTRIC PARALLEL BARSK925164ELECTRIC STAND-IN TABLEK924093ELECTRIC HI LO TILT TABLEK923998MIDLAND TILT TABLEK923973SPACE BASE ELECTRIC TILT TABLEK924002MIDLAND THREE SECTION P.T. TABLE W/ DRAINAGE

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Related Devices (Code: INQ)

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.

K960334CARDON PHYSICAL THERAPY TABLE MODEL R27116Cardon Rehabilitation Products, Inc.K960336CARDON PHYSICAL THERAPY TABLE MODEL R27645Cardon Rehabilitation Products, Inc.K960332CARDON PHYSICAL THERAPY TABLE MODEL R28598Cardon Rehabilitation Products, Inc.K960196TRI W-G, INC TABLE, TILT/EXAM/TREATMENT MODEL 777Tri W-G, Inc.K953621EVT-3300U.S. Table, Inc.K953622PTT 6200 ELEVATION THERAPY TABLEU.S. Table, Inc.

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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