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FDA 510(k)

MEDIGROUP LS-110 LIGHT SOURCE

K-Number: K823294 · 1983-05-09

ApplicantMedigroup
Decision Date1983-05-09
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

MEDIGROUP LS-110 LIGHT SOURCE is the device name listed in this FDA 510(k) record. The listed applicant is Medigroup. It received FDA 510(k) clearance on 1983-05-09 under 510(k) number K823294. 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 LS-110 LIGHT SOURCE?

MEDIGROUP LS-110 LIGHT SOURCE is a medical device that received FDA 510(k) clearance on 1983-05-09. The listed applicant is Medigroup. The 510(k) number is K823294.

When did MEDIGROUP LS-110 LIGHT SOURCE receive FDA 510(k) clearance?

MEDIGROUP LS-110 LIGHT SOURCE received FDA 510(k) clearance on 1983-05-09, under 510(k) number K823294.

Who is the listed applicant for MEDIGROUP LS-110 LIGHT SOURCE?

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 LS-110 LIGHT SOURCE?

The FDA product code for MEDIGROUP LS-110 LIGHT SOURCE 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.

K823295MEDIGROUP 2.2MM NEEDLESCOPE CANNULA&K823297ST-610 NEEDLESCOPE STERILIZATION TRAYK823293MEDIGROUP LG-102 LIGHT GUIDEK823331PC-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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