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FDA 510(k)

BACSTOP FILTER IRRIGATION SUPPLY KIT

K-Number: K860544 · 1986-04-04

Decision Date1986-04-04
Product CodeKYG
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

BACSTOP FILTER IRRIGATION SUPPLY KIT is the device name listed in this FDA 510(k) record. The listed applicant is Staar Surgical Co.. It received FDA 510(k) clearance on 1986-04-04 under 510(k) number K860544. The device is classified under product code KYG. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BACSTOP FILTER IRRIGATION SUPPLY KIT?

BACSTOP FILTER IRRIGATION SUPPLY KIT is a medical device that received FDA 510(k) clearance on 1986-04-04. The listed applicant is Staar Surgical Co.. The 510(k) number is K860544.

When did BACSTOP FILTER IRRIGATION SUPPLY KIT receive FDA 510(k) clearance?

BACSTOP FILTER IRRIGATION SUPPLY KIT received FDA 510(k) clearance on 1986-04-04, under 510(k) number K860544.

Who is the listed applicant for BACSTOP FILTER IRRIGATION SUPPLY KIT?

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

What is the FDA product code for BACSTOP FILTER IRRIGATION SUPPLY KIT?

The FDA product code for BACSTOP FILTER IRRIGATION SUPPLY KIT is KYG.

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 Staar Surgical Co. 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 22 devices →

Related Devices (Code: KYG)

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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