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FDA 510(k)

LIGHT, SURGICAL ACCESSORIES

K-Number: K882132 · 1988-06-15

Decision Date1988-06-15
Product CodeFTA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LIGHT, SURGICAL ACCESSORIES is the device name listed in this FDA 510(k) record. The listed applicant is Charles Polo & Co., Inc.. It received FDA 510(k) clearance on 1988-06-15 under 510(k) number K882132. 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 LIGHT, SURGICAL ACCESSORIES?

LIGHT, SURGICAL ACCESSORIES is a medical device that received FDA 510(k) clearance on 1988-06-15. The listed applicant is Charles Polo & Co., Inc.. The 510(k) number is K882132.

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

LIGHT, SURGICAL ACCESSORIES received FDA 510(k) clearance on 1988-06-15, under 510(k) number K882132.

Who is the listed applicant for LIGHT, SURGICAL ACCESSORIES?

The FDA 510(k) record lists Charles Polo & Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LIGHT, SURGICAL ACCESSORIES?

The FDA product code for LIGHT, SURGICAL ACCESSORIES 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 Charles Polo & Co., 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.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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