FLEXTITIP STYLETTE
K-Number: K950380 · 1995-02-10
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Device Summary
Frequently Asked Questions
What is the FLEXTITIP STYLETTE?
FLEXTITIP STYLETTE is a medical device that received FDA 510(k) clearance on 1995-02-10. The listed applicant is Polamedco, Inc.. The 510(k) number is K950380.
When did FLEXTITIP STYLETTE receive FDA 510(k) clearance?
FLEXTITIP STYLETTE received FDA 510(k) clearance on 1995-02-10, under 510(k) number K950380.
Who is the listed applicant for FLEXTITIP STYLETTE?
The FDA 510(k) record lists Polamedco, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FLEXTITIP STYLETTE?
The FDA product code for FLEXTITIP STYLETTE is BSR.
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 Polamedco, 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: BSR)
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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