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FDA 510(k)

MEDLINE'S EXAMIN, OPERATING ROOM/SURG LIGHTS/LAMPS

K-Number: K931675 · 1994-02-22

ApplicantMedline Industries, Inc.
Decision Date1994-02-22
Product CodeFTD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MEDLINE'S EXAMIN, OPERATING ROOM/SURG LIGHTS/LAMPS is the device name listed in this FDA 510(k) record. The listed applicant is Medline Industries, Inc.. It received FDA 510(k) clearance on 1994-02-22 under 510(k) number K931675. The device is classified under product code FTD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDLINE'S EXAMIN, OPERATING ROOM/SURG LIGHTS/LAMPS?

MEDLINE'S EXAMIN, OPERATING ROOM/SURG LIGHTS/LAMPS is a medical device that received FDA 510(k) clearance on 1994-02-22. The listed applicant is Medline Industries, Inc.. The 510(k) number is K931675.

When did MEDLINE'S EXAMIN, OPERATING ROOM/SURG LIGHTS/LAMPS receive FDA 510(k) clearance?

MEDLINE'S EXAMIN, OPERATING ROOM/SURG LIGHTS/LAMPS received FDA 510(k) clearance on 1994-02-22, under 510(k) number K931675.

Who is the listed applicant for MEDLINE'S EXAMIN, OPERATING ROOM/SURG LIGHTS/LAMPS?

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

What is the FDA product code for MEDLINE'S EXAMIN, OPERATING ROOM/SURG LIGHTS/LAMPS?

The FDA product code for MEDLINE'S EXAMIN, OPERATING ROOM/SURG LIGHTS/LAMPS is FTD.

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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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