OPTILINE, CARLO BELLINI, EXPLOREFLEX, STRATFORD & TITINIFLEX
K-Number: K943236 · 1994-08-02
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Device Summary
Frequently Asked Questions
What is the OPTILINE, CARLO BELLINI, EXPLOREFLEX, STRATFORD & TITINIFLEX?
OPTILINE, CARLO BELLINI, EXPLOREFLEX, STRATFORD & TITINIFLEX is a medical device that received FDA 510(k) clearance on 1994-08-02. The listed applicant is Optiline Imports and Trade, Inc.. The 510(k) number is K943236.
When did OPTILINE, CARLO BELLINI, EXPLOREFLEX, STRATFORD & TITINIFLEX receive FDA 510(k) clearance?
OPTILINE, CARLO BELLINI, EXPLOREFLEX, STRATFORD & TITINIFLEX received FDA 510(k) clearance on 1994-08-02, under 510(k) number K943236.
Who is the listed applicant for OPTILINE, CARLO BELLINI, EXPLOREFLEX, STRATFORD & TITINIFLEX?
The FDA 510(k) record lists Optiline Imports and Trade, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OPTILINE, CARLO BELLINI, EXPLOREFLEX, STRATFORD & TITINIFLEX?
The FDA product code for OPTILINE, CARLO BELLINI, EXPLOREFLEX, STRATFORD & TITINIFLEX is HQZ.
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.
Related Devices (Code: HQZ)
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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