SOFT LENS FOLDING BLOCK
K-Number: K891487 · 1989-08-15
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Device Summary
Frequently Asked Questions
What is the SOFT LENS FOLDING BLOCK?
SOFT LENS FOLDING BLOCK is a medical device that received FDA 510(k) clearance on 1989-08-15. The listed applicant is Western Medical Products, Inc.. The 510(k) number is K891487.
When did SOFT LENS FOLDING BLOCK receive FDA 510(k) clearance?
SOFT LENS FOLDING BLOCK received FDA 510(k) clearance on 1989-08-15, under 510(k) number K891487.
Who is the listed applicant for SOFT LENS FOLDING BLOCK?
The FDA 510(k) record lists Western Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SOFT LENS FOLDING BLOCK?
The FDA product code for SOFT LENS FOLDING BLOCK is HNR.
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 Western Medical Products, 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: HNR)
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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