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FDA 510(k)

STAIRMASTER MODEL 6000 ERGOMETER

K-Number: K912140 · 1991-12-17

ApplicantTri-Tech, Inc.
Decision Date1991-12-17
Product CodeISD
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

STAIRMASTER MODEL 6000 ERGOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Tri-Tech, Inc.. It received FDA 510(k) clearance on 1991-12-17 under 510(k) number K912140. The device is classified under product code ISD. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STAIRMASTER MODEL 6000 ERGOMETER?

STAIRMASTER MODEL 6000 ERGOMETER is a medical device that received FDA 510(k) clearance on 1991-12-17. The listed applicant is Tri-Tech, Inc.. The 510(k) number is K912140.

When did STAIRMASTER MODEL 6000 ERGOMETER receive FDA 510(k) clearance?

STAIRMASTER MODEL 6000 ERGOMETER received FDA 510(k) clearance on 1991-12-17, under 510(k) number K912140.

Who is the listed applicant for STAIRMASTER MODEL 6000 ERGOMETER?

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

What is the FDA product code for STAIRMASTER MODEL 6000 ERGOMETER?

The FDA product code for STAIRMASTER MODEL 6000 ERGOMETER is ISD.

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Other records listing Tri-Tech, 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.

K971111TRI-TECH INC., EVACUATED BLOOD COLLECTION TUBE, GRAY STOPPERK952246TRI-TECHIN. CUSTOM BLOOD AND/OR URINE TRANSPORT KITK922343TRI-TECH INC. CUSTOM SEXUAL ASSAULT KITK922342TRI-TECH INC. CUSTOM BLOOD ALCOHOLK912058GAUNTLET STAIR CLIMBERK9120574000 PT EXERCISE SYSTEM

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Related Devices (Code: ISD)

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.

K202979MR Egometer Pedal, MR Ergometer Push/Pull, MR Ergometer Up/Down, MR Ergometer Dorsal Ankle Flex, MR Ergometer Pedal UltraLode B.V.K183296REAL Immersive SystemPenumbra, Inc.K112121ERGOSELECT/GEErgoline GmbHK080545ACTITRAINERActigraph, LLCK053078ERGOSELECT 100 K/P, ERGOSELECT 200 K/PErgoline GmbHK990866QUINTON MEDTRACK CR PLUS TREADMILLQuinton, 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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