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FDA 510(k)

DISPOSABLE TEMPERATURE PROBE

K-Number: K770353 · 1977-03-16

Decision Date1977-03-16
Product CodeKPD
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE TEMPERATURE PROBE is the device name listed in this FDA 510(k) record. The listed applicant is Inhal-O-Tech Medical Plastic. It received FDA 510(k) clearance on 1977-03-16 under 510(k) number K770353. The device is classified under product code KPD. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOSABLE TEMPERATURE PROBE?

DISPOSABLE TEMPERATURE PROBE is a medical device that received FDA 510(k) clearance on 1977-03-16. The listed applicant is Inhal-O-Tech Medical Plastic. The 510(k) number is K770353.

When did DISPOSABLE TEMPERATURE PROBE receive FDA 510(k) clearance?

DISPOSABLE TEMPERATURE PROBE received FDA 510(k) clearance on 1977-03-16, under 510(k) number K770353.

Who is the listed applicant for DISPOSABLE TEMPERATURE PROBE?

The FDA 510(k) record lists Inhal-O-Tech Medical Plastic as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DISPOSABLE TEMPERATURE PROBE?

The FDA product code for DISPOSABLE TEMPERATURE PROBE is KPD.

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.

Other records listing Inhal-O-Tech Medical Plastic 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.

View all 7 devices →

Related Devices (Code: KPD)

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.

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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