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FDA 510(k)

HILO TABLE

K-Number: K933621 · 1994-01-07

ApplicantSpinalight, Inc.
Decision Date1994-01-07
Product CodeINQ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

HILO TABLE is the device name listed in this FDA 510(k) record. The listed applicant is Spinalight, Inc.. It received FDA 510(k) clearance on 1994-01-07 under 510(k) number K933621. 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 HILO TABLE?

HILO TABLE is a medical device that received FDA 510(k) clearance on 1994-01-07. The listed applicant is Spinalight, Inc.. The 510(k) number is K933621.

When did HILO TABLE receive FDA 510(k) clearance?

HILO TABLE received FDA 510(k) clearance on 1994-01-07, under 510(k) number K933621.

Who is the listed applicant for HILO TABLE?

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

What is the FDA product code for HILO TABLE?

The FDA product code for HILO TABLE is INQ.

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Other records listing Spinalight, Inc. 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.

K172536Atlas Percussion Adjusting InstrumentK001476TORQUE INSTRUMENT, MODEL 8500K955540HAND HELD ATLAS INSTRUMENTK946258MODEL 8000 ATLAS C-1 ORTHOGONAL ADJUSTING INSTRUMENTK945954MODELS 4100 AND 4300 MULTITHERAPYK933622FLEXION DISTRACTION TABLE

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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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