NON-PRESSURE AUTOCLAVE FOR STERILIZATION
K-Number: K823457 · 1983-02-23
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Device Summary
Frequently Asked Questions
What is the NON-PRESSURE AUTOCLAVE FOR STERILIZATION?
NON-PRESSURE AUTOCLAVE FOR STERILIZATION is a medical device that received FDA 510(k) clearance on 1983-02-23. The listed applicant is Interdent, Inc.. The 510(k) number is K823457.
When did NON-PRESSURE AUTOCLAVE FOR STERILIZATION receive FDA 510(k) clearance?
NON-PRESSURE AUTOCLAVE FOR STERILIZATION received FDA 510(k) clearance on 1983-02-23, under 510(k) number K823457.
Who is the listed applicant for NON-PRESSURE AUTOCLAVE FOR STERILIZATION?
The FDA 510(k) record lists Interdent, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NON-PRESSURE AUTOCLAVE FOR STERILIZATION?
The FDA product code for NON-PRESSURE AUTOCLAVE FOR STERILIZATION is FLE.
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 Interdent, 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: FLE)
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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