Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

MIDMARK SURGICAL LIGHTING SYSTEMS

K-Number: K930686 · 1993-07-30

ApplicantMidmark Corp.
Decision Date1993-07-30
Product CodeFSQ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MIDMARK SURGICAL LIGHTING SYSTEMS is the device name listed in this FDA 510(k) record. The listed applicant is Midmark Corp.. It received FDA 510(k) clearance on 1993-07-30 under 510(k) number K930686. The device is classified under product code FSQ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MIDMARK SURGICAL LIGHTING SYSTEMS?

MIDMARK SURGICAL LIGHTING SYSTEMS is a medical device that received FDA 510(k) clearance on 1993-07-30. The listed applicant is Midmark Corp.. The 510(k) number is K930686.

When did MIDMARK SURGICAL LIGHTING SYSTEMS receive FDA 510(k) clearance?

MIDMARK SURGICAL LIGHTING SYSTEMS received FDA 510(k) clearance on 1993-07-30, under 510(k) number K930686.

Who is the listed applicant for MIDMARK SURGICAL LIGHTING SYSTEMS?

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

What is the FDA product code for MIDMARK SURGICAL LIGHTING SYSTEMS?

The FDA product code for MIDMARK SURGICAL LIGHTING SYSTEMS is FSQ.

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 Midmark Corp. 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 31 devices →

Related Devices (Code: FSQ)

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.

↑