NEZHAT-DORSEY THERMAL RETENTION SYSTEM
K-Number: K951300 · 1995-06-20
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Device Summary
Frequently Asked Questions
What is the NEZHAT-DORSEY THERMAL RETENTION SYSTEM?
NEZHAT-DORSEY THERMAL RETENTION SYSTEM is a medical device that received FDA 510(k) clearance on 1995-06-20. The listed applicant is American Hydro-Surgical Instruments, Inc.. The 510(k) number is K951300.
When did NEZHAT-DORSEY THERMAL RETENTION SYSTEM receive FDA 510(k) clearance?
NEZHAT-DORSEY THERMAL RETENTION SYSTEM received FDA 510(k) clearance on 1995-06-20, under 510(k) number K951300.
Who is the listed applicant for NEZHAT-DORSEY THERMAL RETENTION SYSTEM?
The FDA 510(k) record lists American Hydro-Surgical Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NEZHAT-DORSEY THERMAL RETENTION SYSTEM?
The FDA product code for NEZHAT-DORSEY THERMAL RETENTION SYSTEM is LHC.
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 American Hydro-Surgical Instruments, 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: LHC)
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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