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FDA 510(k)

BAUSCH & LOMB2 SENSITIVE EYES MULTI-PURPOSE SOLUTION

K-Number: K973921 · 1998-01-12

ApplicantBausch & Lomb, Inc.
Decision Date1998-01-12
Product CodeLPN
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

BAUSCH & LOMB2 SENSITIVE EYES MULTI-PURPOSE SOLUTION is the device name listed in this FDA 510(k) record. The listed applicant is Bausch & Lomb, Inc.. It received FDA 510(k) clearance on 1998-01-12 under 510(k) number K973921. 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 BAUSCH & LOMB2 SENSITIVE EYES MULTI-PURPOSE SOLUTION?

BAUSCH & LOMB2 SENSITIVE EYES MULTI-PURPOSE SOLUTION is a medical device that received FDA 510(k) clearance on 1998-01-12. The listed applicant is Bausch & Lomb, Inc.. The 510(k) number is K973921.

When did BAUSCH & LOMB2 SENSITIVE EYES MULTI-PURPOSE SOLUTION receive FDA 510(k) clearance?

BAUSCH & LOMB2 SENSITIVE EYES MULTI-PURPOSE SOLUTION received FDA 510(k) clearance on 1998-01-12, under 510(k) number K973921.

Who is the listed applicant for BAUSCH & LOMB2 SENSITIVE EYES MULTI-PURPOSE SOLUTION?

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

What is the FDA product code for BAUSCH & LOMB2 SENSITIVE EYES MULTI-PURPOSE SOLUTION?

The FDA product code for BAUSCH & LOMB2 SENSITIVE EYES MULTI-PURPOSE SOLUTION is LPN.

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Other records listing Bausch & Lomb, 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.

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Related Devices (Code: LPN)

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.

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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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