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FDA 510(k)

LEVELSENS - FLEXIBLE, MODEL 201110, LEVELSENS - RIGID, MODEL 201070

K-Number: K992857 · 1999-11-10

ApplicantRocky Mountain Research, Inc.
Decision Date1999-11-10
Product CodeDTW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

LEVELSENS - FLEXIBLE, MODEL 201110, LEVELSENS - RIGID, MODEL 201070 is the device name listed in this FDA 510(k) record. The listed applicant is Rocky Mountain Research, Inc.. It received FDA 510(k) clearance on 1999-11-10 under 510(k) number K992857. The device is classified under product code DTW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LEVELSENS - FLEXIBLE, MODEL 201110, LEVELSENS - RIGID, MODEL 201070?

LEVELSENS - FLEXIBLE, MODEL 201110, LEVELSENS - RIGID, MODEL 201070 is a medical device that received FDA 510(k) clearance on 1999-11-10. The listed applicant is Rocky Mountain Research, Inc.. The 510(k) number is K992857.

When did LEVELSENS - FLEXIBLE, MODEL 201110, LEVELSENS - RIGID, MODEL 201070 receive FDA 510(k) clearance?

LEVELSENS - FLEXIBLE, MODEL 201110, LEVELSENS - RIGID, MODEL 201070 received FDA 510(k) clearance on 1999-11-10, under 510(k) number K992857.

Who is the listed applicant for LEVELSENS - FLEXIBLE, MODEL 201110, LEVELSENS - RIGID, MODEL 201070?

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

What is the FDA product code for LEVELSENS - FLEXIBLE, MODEL 201110, LEVELSENS - RIGID, MODEL 201070?

The FDA product code for LEVELSENS - FLEXIBLE, MODEL 201110, LEVELSENS - RIGID, MODEL 201070 is DTW.

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Other records listing Rocky Mountain Research, Inc. as applicant

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Related Devices (Code: DTW)

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.

K041558STOCKERTIR PURGE CONTROL (APC) SYSTEMStockert Instrumente GmbHK955152STOCKERT S3 UPS, LVL CTRL BUBB. DET., DUAL PRESS. CTRL., TEMP MONT., TIMERStoeckert InstrumenteK910599CARDIOPULMONARY BYPASS LEVEL SENSING MONITORJtl Medical Corp.K924354STOCKERT CAPS LOW LEVEL DETECT II/BUBBLE MONITORSorin Biomedica, Fiat, USA, Inc.K915337CAPIOX LEVEL ALARMTerumo Medical Corp.K900910COBE AIR EMBOLI PROTECTION SYSTEM (AEPS)Cobe Laboratories, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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