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FDA 510(k)

HATCHER STONE EXTRACTOR - DISPOSABLE CATHETER

K-Number: K862949 · 1986-10-31

Decision Date1986-10-31
Product CodeLQR
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

HATCHER STONE EXTRACTOR - DISPOSABLE CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Oscor Medical Corp.. It received FDA 510(k) clearance on 1986-10-31 under 510(k) number K862949. The device is classified under product code LQR. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HATCHER STONE EXTRACTOR - DISPOSABLE CATHETER?

HATCHER STONE EXTRACTOR - DISPOSABLE CATHETER is a medical device that received FDA 510(k) clearance on 1986-10-31. The listed applicant is Oscor Medical Corp.. The 510(k) number is K862949.

When did HATCHER STONE EXTRACTOR - DISPOSABLE CATHETER receive FDA 510(k) clearance?

HATCHER STONE EXTRACTOR - DISPOSABLE CATHETER received FDA 510(k) clearance on 1986-10-31, under 510(k) number K862949.

Who is the listed applicant for HATCHER STONE EXTRACTOR - DISPOSABLE CATHETER?

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

What is the FDA product code for HATCHER STONE EXTRACTOR - DISPOSABLE CATHETER?

The FDA product code for HATCHER STONE EXTRACTOR - DISPOSABLE CATHETER is LQR.

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 Oscor Medical 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: LQR)

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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