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FDA 510(k)

MEDIGROUP LG-102 LIGHT GUIDE

K-Number: K823293 · 1983-05-05

ApplicantMedigroup
Decision Date1983-05-05
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

MEDIGROUP LG-102 LIGHT GUIDE is the device name listed in this FDA 510(k) record. The listed applicant is Medigroup. It received FDA 510(k) clearance on 1983-05-05 under 510(k) number K823293. The device is classified under product code HET. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDIGROUP LG-102 LIGHT GUIDE?

MEDIGROUP LG-102 LIGHT GUIDE is a medical device that received FDA 510(k) clearance on 1983-05-05. The listed applicant is Medigroup. The 510(k) number is K823293.

When did MEDIGROUP LG-102 LIGHT GUIDE receive FDA 510(k) clearance?

MEDIGROUP LG-102 LIGHT GUIDE received FDA 510(k) clearance on 1983-05-05, under 510(k) number K823293.

Who is the listed applicant for MEDIGROUP LG-102 LIGHT GUIDE?

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

What is the FDA product code for MEDIGROUP LG-102 LIGHT GUIDE?

The FDA product code for MEDIGROUP LG-102 LIGHT GUIDE is HET.

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Other records listing Medigroup 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.

K823294MEDIGROUP LS-110 LIGHT SOURCEK823295MEDIGROUP 2.2MM NEEDLESCOPE CANNULA&K823297ST-610 NEEDLESCOPE STERILIZATION TRAYK823331PC-204 TUNNELORK823390PC 201A LOCKING SLEEVEK823303QUILL CATHETER GUIDE

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Related Devices (Code: HET)

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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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