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FDA 510(k)

POWERMATIC MAT PLATFORM

K-Number: K933578 · 1993-11-05

ApplicantMedical Device Inspection Co., Inc.
Decision Date1993-11-05
Product CodeINQ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

POWERMATIC MAT PLATFORM is the device name listed in this FDA 510(k) record. The listed applicant is Medical Device Inspection Co., Inc.. It received FDA 510(k) clearance on 1993-11-05 under 510(k) number K933578. 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 POWERMATIC MAT PLATFORM?

POWERMATIC MAT PLATFORM is a medical device that received FDA 510(k) clearance on 1993-11-05. The listed applicant is Medical Device Inspection Co., Inc.. The 510(k) number is K933578.

When did POWERMATIC MAT PLATFORM receive FDA 510(k) clearance?

POWERMATIC MAT PLATFORM received FDA 510(k) clearance on 1993-11-05, under 510(k) number K933578.

Who is the listed applicant for POWERMATIC MAT PLATFORM?

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

What is the FDA product code for POWERMATIC MAT PLATFORM?

The FDA product code for POWERMATIC MAT PLATFORM is INQ.

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Other records listing Medical Device Inspection Co., 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.

K945826J & J I-330 SERIES PHYSIOLOGICAL MONITORING & BIOFEEDBACK INSTUMENT AND USE SOFTWARE APPLICATIONSK932072JARIT SURGICAL INSTRUMENTSK931594THERA-TURN CM-1000 MATTRESS OVERLAY SYSTEMK933581POWERMATIC TREATMENT TABLEK933580POWER WORK TABLEK933577POWERMATIC EXAMINATION 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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