TISSUE EXPANDERS FOR RECONSTRUC-SURGERY 3600
K-Number: K845036 · 1985-06-26
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Device Summary
Frequently Asked Questions
What is the TISSUE EXPANDERS FOR RECONSTRUC-SURGERY 3600?
TISSUE EXPANDERS FOR RECONSTRUC-SURGERY 3600 is a medical device that received FDA 510(k) clearance on 1985-06-26. The listed applicant is Progress Mankind Technology. The 510(k) number is K845036.
When did TISSUE EXPANDERS FOR RECONSTRUC-SURGERY 3600 receive FDA 510(k) clearance?
TISSUE EXPANDERS FOR RECONSTRUC-SURGERY 3600 received FDA 510(k) clearance on 1985-06-26, under 510(k) number K845036.
Who is the listed applicant for TISSUE EXPANDERS FOR RECONSTRUC-SURGERY 3600?
The FDA 510(k) record lists Progress Mankind Technology as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TISSUE EXPANDERS FOR RECONSTRUC-SURGERY 3600?
The FDA product code for TISSUE EXPANDERS FOR RECONSTRUC-SURGERY 3600 is LCJ.
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 Progress Mankind Technology 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: LCJ)
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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