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FDA 510(k)

WOUND DRAINAGE HOLDER

K-Number: K973183 · 1998-01-23

ApplicantR & D Medical Products, Inc.
Decision Date1998-01-23
Product CodeKGZ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

WOUND DRAINAGE HOLDER is the device name listed in this FDA 510(k) record. The listed applicant is R & D Medical Products, Inc.. It received FDA 510(k) clearance on 1998-01-23 under 510(k) number K973183. The device is classified under product code KGZ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WOUND DRAINAGE HOLDER?

WOUND DRAINAGE HOLDER is a medical device that received FDA 510(k) clearance on 1998-01-23. The listed applicant is R & D Medical Products, Inc.. The 510(k) number is K973183.

When did WOUND DRAINAGE HOLDER receive FDA 510(k) clearance?

WOUND DRAINAGE HOLDER received FDA 510(k) clearance on 1998-01-23, under 510(k) number K973183.

Who is the listed applicant for WOUND DRAINAGE HOLDER?

The FDA 510(k) record lists R & D Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WOUND DRAINAGE HOLDER?

The FDA product code for WOUND DRAINAGE HOLDER is KGZ.

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.

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Other records listing R & D Medical Products, Inc. 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.

K111555CIRCUMAURAL ADHESIVE REPLACEMENTK092744NEONATAL ECG ELECTRODE, M203KENK001117COMFORT STIM

Related Devices (Code: KGZ)

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.

K022306AART SILICONE TUBINGAesthetic and Reconstructive Technologies, Inc.K974295BYRON MEDICAL ASPIRATION AND INFILTRATION/IRRIGATION TUBINGByron MedicalK955433DURALASTIC SILICONE TUBINGAllied Biomedical Corp.K942315NAVARRE PERCUTANEOUS ACCESS SETNavarre Biomedical , Ltd.K896087PALESTRANT IRRIGATION AND DRAINAGE SETNorth American Instrument Corp.K895041OPTICAL CATHETER(TM) INTRODUCER SETSMedical Dynamics, Inc.

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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