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FDA 510(k)

SUTURE REMOVAL WOUND CLOSURE-INSTRU-

K-Number: K834367 · 1984-05-30

ApplicantSterling Multi-Products, Inc.
Decision Date1984-05-30
Product CodeHTD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SUTURE REMOVAL WOUND CLOSURE-INSTRU- is the device name listed in this FDA 510(k) record. The listed applicant is Sterling Multi-Products, Inc.. It received FDA 510(k) clearance on 1984-05-30 under 510(k) number K834367. The device is classified under product code HTD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUTURE REMOVAL WOUND CLOSURE-INSTRU-?

SUTURE REMOVAL WOUND CLOSURE-INSTRU- is a medical device that received FDA 510(k) clearance on 1984-05-30. The listed applicant is Sterling Multi-Products, Inc.. The 510(k) number is K834367.

When did SUTURE REMOVAL WOUND CLOSURE-INSTRU- receive FDA 510(k) clearance?

SUTURE REMOVAL WOUND CLOSURE-INSTRU- received FDA 510(k) clearance on 1984-05-30, under 510(k) number K834367.

Who is the listed applicant for SUTURE REMOVAL WOUND CLOSURE-INSTRU-?

The FDA 510(k) record lists Sterling Multi-Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SUTURE REMOVAL WOUND CLOSURE-INSTRU-?

The FDA product code for SUTURE REMOVAL WOUND CLOSURE-INSTRU- is HTD.

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Related Devices (Code: HTD)

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.

K051281THE NEEDLE CATCHERE.D.Medical , Ltd.K974595CUSHING BAYONET, INSULATED BIPOLAR FORCEPTitan Mfg., Inc.K974594SEMKIN BIPOLAR FORCEPTitan Mfg., Inc.K974593SEMKIN INSULATED BIPOLAR FORCEPTitan Mfg., Inc.K913964MARLOW/REDDICK LAPAROSCOPIC GRASPING FORCEPSMarlo Surgical TechnologyK911180CLAW (5MM/10MM) ATRAUMATIC GRASP/MICRO FORCEPSNorthgate Technologies, 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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