THERMO SET ELECTRONIC TEM. CONTROLLER
K-Number: K780888 · 1978-06-28
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Device Summary
Frequently Asked Questions
What is the THERMO SET ELECTRONIC TEM. CONTROLLER?
THERMO SET ELECTRONIC TEM. CONTROLLER is a medical device that received FDA 510(k) clearance on 1978-06-28. The listed applicant is Gilford Instrument Laboratories, Inc.. The 510(k) number is K780888.
When did THERMO SET ELECTRONIC TEM. CONTROLLER receive FDA 510(k) clearance?
THERMO SET ELECTRONIC TEM. CONTROLLER received FDA 510(k) clearance on 1978-06-28, under 510(k) number K780888.
Who is the listed applicant for THERMO SET ELECTRONIC TEM. CONTROLLER?
The FDA 510(k) record lists Gilford Instrument Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for THERMO SET ELECTRONIC TEM. CONTROLLER?
The FDA product code for THERMO SET ELECTRONIC TEM. CONTROLLER is JRI.
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 Gilford Instrument Laboratories, 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.
Related Devices (Code: JRI)
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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