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FDA 510(k)

ALCON MULTI-PURPOSE SOLUTION

K-Number: K071236 · 2007-12-12

ApplicantAlcon, Inc.
Decision Date2007-12-12
Product CodeLPN
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

ALCON MULTI-PURPOSE SOLUTION is the device name listed in this FDA 510(k) record. The listed applicant is Alcon, Inc.. It received FDA 510(k) clearance on 2007-12-12 under 510(k) number K071236. The device is classified under product code LPN. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ALCON MULTI-PURPOSE SOLUTION?

ALCON MULTI-PURPOSE SOLUTION is a medical device that received FDA 510(k) clearance on 2007-12-12. The listed applicant is Alcon, Inc.. The 510(k) number is K071236.

When did ALCON MULTI-PURPOSE SOLUTION receive FDA 510(k) clearance?

ALCON MULTI-PURPOSE SOLUTION received FDA 510(k) clearance on 2007-12-12, under 510(k) number K071236.

Who is the listed applicant for ALCON MULTI-PURPOSE SOLUTION?

The FDA 510(k) record lists Alcon, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ALCON MULTI-PURPOSE SOLUTION?

The FDA product code for ALCON MULTI-PURPOSE SOLUTION is LPN.

Related Clinical Trials

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Other records listing Alcon, 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.

K040231INTELIPORT OCCLUDING DEVICEK031193SOFT (HYDROPHILIC) CONTACT LENS CARE SOLUTION

Related Devices (Code: LPN)

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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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