FLEXT-THERM
K-Number: K781916 · 1979-02-02
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Device Summary
Frequently Asked Questions
What is the FLEXT-THERM?
FLEXT-THERM is a medical device that received FDA 510(k) clearance on 1979-02-02. The listed applicant is E-Z-Em, Inc.. The 510(k) number is K781916.
When did FLEXT-THERM receive FDA 510(k) clearance?
FLEXT-THERM received FDA 510(k) clearance on 1979-02-02, under 510(k) number K781916.
Who is the listed applicant for FLEXT-THERM?
The FDA 510(k) record lists E-Z-Em, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FLEXT-THERM?
The FDA product code for FLEXT-THERM is KXZ.
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 E-Z-Em, 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: KXZ)
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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