PS2 BRAND MAMMAPLASTY
K-Number: K860912 · 1986-03-24
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Device Summary
Frequently Asked Questions
What is the PS2 BRAND MAMMAPLASTY?
PS2 BRAND MAMMAPLASTY is a medical device that received FDA 510(k) clearance on 1986-03-24. The listed applicant is Professional Services For Surgeons, Ltd.. The 510(k) number is K860912.
When did PS2 BRAND MAMMAPLASTY receive FDA 510(k) clearance?
PS2 BRAND MAMMAPLASTY received FDA 510(k) clearance on 1986-03-24, under 510(k) number K860912.
Who is the listed applicant for PS2 BRAND MAMMAPLASTY?
The FDA 510(k) record lists Professional Services For Surgeons, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PS2 BRAND MAMMAPLASTY?
The FDA product code for PS2 BRAND MAMMAPLASTY is FTY.
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 Professional Services For Surgeons, Ltd. 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: FTY)
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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