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FDA 510(k)

KENLOR H. PYLORI CONTROL SERUM

K-Number: K964014 · 1997-03-03

ApplicantKenlor Industries, Inc.
Decision Date1997-03-03
Product CodeLYR
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

KENLOR H. PYLORI CONTROL SERUM is the device name listed in this FDA 510(k) record. The listed applicant is Kenlor Industries, Inc.. It received FDA 510(k) clearance on 1997-03-03 under 510(k) number K964014. The device is classified under product code LYR. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KENLOR H. PYLORI CONTROL SERUM?

KENLOR H. PYLORI CONTROL SERUM is a medical device that received FDA 510(k) clearance on 1997-03-03. The listed applicant is Kenlor Industries, Inc.. The 510(k) number is K964014.

When did KENLOR H. PYLORI CONTROL SERUM receive FDA 510(k) clearance?

KENLOR H. PYLORI CONTROL SERUM received FDA 510(k) clearance on 1997-03-03, under 510(k) number K964014.

Who is the listed applicant for KENLOR H. PYLORI CONTROL SERUM?

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

What is the FDA product code for KENLOR H. PYLORI CONTROL SERUM?

The FDA product code for KENLOR H. PYLORI CONTROL SERUM is LYR.

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Other records listing Kenlor Industries, Inc. as applicant

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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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