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FDA 510(k)

THERMOGRAPH, MEDICAL

K-Number: K760999 · 1976-11-19

ApplicantHoneywell, Inc.
Decision Date1976-11-19
Product CodeIYM
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

THERMOGRAPH, MEDICAL is the device name listed in this FDA 510(k) record. The listed applicant is Honeywell, Inc.. It received FDA 510(k) clearance on 1976-11-19 under 510(k) number K760999. The device is classified under product code IYM. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THERMOGRAPH, MEDICAL?

THERMOGRAPH, MEDICAL is a medical device that received FDA 510(k) clearance on 1976-11-19. The listed applicant is Honeywell, Inc.. The 510(k) number is K760999.

When did THERMOGRAPH, MEDICAL receive FDA 510(k) clearance?

THERMOGRAPH, MEDICAL received FDA 510(k) clearance on 1976-11-19, under 510(k) number K760999.

Who is the listed applicant for THERMOGRAPH, MEDICAL?

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

What is the FDA product code for THERMOGRAPH, MEDICAL?

The FDA product code for THERMOGRAPH, MEDICAL is IYM.

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Other records listing Honeywell, Inc. as applicant

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Related Devices (Code: IYM)

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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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