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FDA 510(k)

RTM REHABILITATION TREADMILL, MODEL #945-200

K-Number: K930261 · 1993-05-26

ApplicantBiodan Medical Systems, Ltd.
Decision Date1993-05-26
Product CodeIOL
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

RTM REHABILITATION TREADMILL, MODEL #945-200 is the device name listed in this FDA 510(k) record. The listed applicant is Biodan Medical Systems, Ltd.. It received FDA 510(k) clearance on 1993-05-26 under 510(k) number K930261. The device is classified under product code IOL. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RTM REHABILITATION TREADMILL, MODEL #945-200?

RTM REHABILITATION TREADMILL, MODEL #945-200 is a medical device that received FDA 510(k) clearance on 1993-05-26. The listed applicant is Biodan Medical Systems, Ltd.. The 510(k) number is K930261.

When did RTM REHABILITATION TREADMILL, MODEL #945-200 receive FDA 510(k) clearance?

RTM REHABILITATION TREADMILL, MODEL #945-200 received FDA 510(k) clearance on 1993-05-26, under 510(k) number K930261.

Who is the listed applicant for RTM REHABILITATION TREADMILL, MODEL #945-200?

The FDA 510(k) record lists Biodan Medical Systems, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RTM REHABILITATION TREADMILL, MODEL #945-200?

The FDA product code for RTM REHABILITATION TREADMILL, MODEL #945-200 is IOL.

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Other records listing Biodan Medical Systems, Ltd. 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.

K932153THYROID UPTAKE SYSTEM & ATOMLAB 950 MED. SPECTROMEK930262TREATMENT TABLE, MODEL #825-100K930259TRACTION TABLE MODEL #825-200K926083NUCLEAR PATIENT SANNING TABLES, VARIOUS TYPESK926082CARDIAC STRESS TABLE, 056-180/UNIV ROLL STRESS ATTK922591UROLOGICAL C-ARM TABLE, MODEL #056-450

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Related Devices (Code: IOL)

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.

K950376PARKER MODEL PMParker Treadmill Co., Inc.K950377PARKER MODEL PEParker Treadmill Co., Inc.K925839TRACKMASTERJas Manufacturing Co., Inc.K904556MANSFIELD CARDIAC ASSIST MODEL 940(TM) IABBoston Scientific CorpK913518TA620 TREADMILL CONTROLLERSiemens Burdick, Inc.K910867T600 TREADMILLSiemens Burdick, 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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