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FDA 510(k)

JOHNLOZ ENDOSCOPY HANDLE

K-Number: K800915 · 1980-05-30

ApplicantEndoscopic Surgical Accessories, Inc.
Decision Date1980-05-30
Product CodeKNS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

JOHNLOZ ENDOSCOPY HANDLE is the device name listed in this FDA 510(k) record. The listed applicant is Endoscopic Surgical Accessories, Inc.. It received FDA 510(k) clearance on 1980-05-30 under 510(k) number K800915. The device is classified under product code KNS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JOHNLOZ ENDOSCOPY HANDLE?

JOHNLOZ ENDOSCOPY HANDLE is a medical device that received FDA 510(k) clearance on 1980-05-30. The listed applicant is Endoscopic Surgical Accessories, Inc.. The 510(k) number is K800915.

When did JOHNLOZ ENDOSCOPY HANDLE receive FDA 510(k) clearance?

JOHNLOZ ENDOSCOPY HANDLE received FDA 510(k) clearance on 1980-05-30, under 510(k) number K800915.

Who is the listed applicant for JOHNLOZ ENDOSCOPY HANDLE?

The FDA 510(k) record lists Endoscopic Surgical Accessories, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for JOHNLOZ ENDOSCOPY HANDLE?

The FDA product code for JOHNLOZ ENDOSCOPY HANDLE is KNS.

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Related Devices (Code: KNS)

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.

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Official Source

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