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FDA 510(k)

CHICK SURGICAL LIGHT

K-Number: K862010 · 1986-06-09

Decision Date1986-06-09
Product CodeFTA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CHICK SURGICAL LIGHT is the device name listed in this FDA 510(k) record. The listed applicant is Professional Medical Products, Inc.. It received FDA 510(k) clearance on 1986-06-09 under 510(k) number K862010. The device is classified under product code FTA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHICK SURGICAL LIGHT?

CHICK SURGICAL LIGHT is a medical device that received FDA 510(k) clearance on 1986-06-09. The listed applicant is Professional Medical Products, Inc.. The 510(k) number is K862010.

When did CHICK SURGICAL LIGHT receive FDA 510(k) clearance?

CHICK SURGICAL LIGHT received FDA 510(k) clearance on 1986-06-09, under 510(k) number K862010.

Who is the listed applicant for CHICK SURGICAL LIGHT?

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

What is the FDA product code for CHICK SURGICAL LIGHT?

The FDA product code for CHICK SURGICAL LIGHT is FTA.

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 Professional Medical Products, Inc. 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 9 devices →

Related Devices (Code: FTA)

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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