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FDA 510(k)

RPI REPLACEMENT HEATING ELEMENTS

K-Number: K020966 · 2002-06-13

ApplicantReplacement Parts Industries, Inc.
Decision Date2002-06-13
Product CodeFMT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

RPI REPLACEMENT HEATING ELEMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Replacement Parts Industries, Inc.. It received FDA 510(k) clearance on 2002-06-13 under 510(k) number K020966. The device is classified under product code FMT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RPI REPLACEMENT HEATING ELEMENTS?

RPI REPLACEMENT HEATING ELEMENTS is a medical device that received FDA 510(k) clearance on 2002-06-13. The listed applicant is Replacement Parts Industries, Inc.. The 510(k) number is K020966.

When did RPI REPLACEMENT HEATING ELEMENTS receive FDA 510(k) clearance?

RPI REPLACEMENT HEATING ELEMENTS received FDA 510(k) clearance on 2002-06-13, under 510(k) number K020966.

Who is the listed applicant for RPI REPLACEMENT HEATING ELEMENTS?

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

What is the FDA product code for RPI REPLACEMENT HEATING ELEMENTS?

The FDA product code for RPI REPLACEMENT HEATING ELEMENTS is FMT.

Related Clinical Trials

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.

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Other records listing Replacement Parts Industries, 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.

K021531RPI REPLACEMENT PHOTOTHERAPY LIGHTSK020219RPI SKIN OR AIR TEMPERATURE PROBE

Related Devices (Code: FMT)

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.

K243606Babyroo TN300Draeger Medical Systems, Inc.K230278Babyroo TN300Draeger Medical Systems, Inc.K213551Giraffe Omnibed Carestation CS1Datex Ohmeda, Inc.K201628Panda iRes Warmer, Giraffe WarmerGE HealthcareK200319HYDRO-TEMP Neonatal Skin Surface Temperature Sensor, HYDRO-TEMP Neonatal Skin Surface Temperature Sensor with Interface CableDeroyal Industries, Inc.K191425Hydro-Temp Neonatal Skin Temperature Probe CoverDeroyal Industries, 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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