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FDA 510(k)

RGP MULTI-PURPOSE SOLUTION ID 100136

K-Number: K000148 · 2000-04-11

Decision Date2000-04-11
Product CodeMRC
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

RGP MULTI-PURPOSE SOLUTION ID 100136 is the device name listed in this FDA 510(k) record. The listed applicant is Alcon Laboratories. It received FDA 510(k) clearance on 2000-04-11 under 510(k) number K000148. The device is classified under product code MRC. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RGP MULTI-PURPOSE SOLUTION ID 100136?

RGP MULTI-PURPOSE SOLUTION ID 100136 is a medical device that received FDA 510(k) clearance on 2000-04-11. The listed applicant is Alcon Laboratories. The 510(k) number is K000148.

When did RGP MULTI-PURPOSE SOLUTION ID 100136 receive FDA 510(k) clearance?

RGP MULTI-PURPOSE SOLUTION ID 100136 received FDA 510(k) clearance on 2000-04-11, under 510(k) number K000148.

Who is the listed applicant for RGP MULTI-PURPOSE SOLUTION ID 100136?

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

What is the FDA product code for RGP MULTI-PURPOSE SOLUTION ID 100136?

The FDA product code for RGP MULTI-PURPOSE SOLUTION ID 100136 is MRC.

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 Alcon Laboratories 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.

View all 47 devices →

Related Devices (Code: MRC)

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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