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FDA 510(k)

WOUND CARE MANAGEMENT KITS

K-Number: K952335 · 1995-06-14

ApplicantContinental Medical Laboratories, Inc.
Decision Date1995-06-14
Product CodeLYY
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

WOUND CARE MANAGEMENT KITS is the device name listed in this FDA 510(k) record. The listed applicant is Continental Medical Laboratories, Inc.. It received FDA 510(k) clearance on 1995-06-14 under 510(k) number K952335. The device is classified under product code LYY. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WOUND CARE MANAGEMENT KITS?

WOUND CARE MANAGEMENT KITS is a medical device that received FDA 510(k) clearance on 1995-06-14. The listed applicant is Continental Medical Laboratories, Inc.. The 510(k) number is K952335.

When did WOUND CARE MANAGEMENT KITS receive FDA 510(k) clearance?

WOUND CARE MANAGEMENT KITS received FDA 510(k) clearance on 1995-06-14, under 510(k) number K952335.

Who is the listed applicant for WOUND CARE MANAGEMENT KITS?

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

What is the FDA product code for WOUND CARE MANAGEMENT KITS?

The FDA product code for WOUND CARE MANAGEMENT KITS is LYY.

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Other records listing Continental Medical Laboratories, 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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