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FDA 510(k)

STIHLER ASTOTHERM IFT 200, IFT 220

K-Number: K882361 · 1988-08-25

ApplicantStihler Electronic, C/O Worldwide Regul. Services
Decision Date1988-08-25
Product CodeLGZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

STIHLER ASTOTHERM IFT 200, IFT 220 is the device name listed in this FDA 510(k) record. The listed applicant is Stihler Electronic, C/O Worldwide Regul. Services. It received FDA 510(k) clearance on 1988-08-25 under 510(k) number K882361. The device is classified under product code LGZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STIHLER ASTOTHERM IFT 200, IFT 220?

STIHLER ASTOTHERM IFT 200, IFT 220 is a medical device that received FDA 510(k) clearance on 1988-08-25. The listed applicant is Stihler Electronic, C/O Worldwide Regul. Services. The 510(k) number is K882361.

When did STIHLER ASTOTHERM IFT 200, IFT 220 receive FDA 510(k) clearance?

STIHLER ASTOTHERM IFT 200, IFT 220 received FDA 510(k) clearance on 1988-08-25, under 510(k) number K882361.

Who is the listed applicant for STIHLER ASTOTHERM IFT 200, IFT 220?

The FDA 510(k) record lists Stihler Electronic, C/O Worldwide Regul. Services as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STIHLER ASTOTHERM IFT 200, IFT 220?

The FDA product code for STIHLER ASTOTHERM IFT 200, IFT 220 is LGZ.

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Related Devices (Code: LGZ)

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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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