Mulhollan Arthroscopic Needle Carrier

FDA 510(k) K834370 · Acufex Microsurgical, Inc.

Substantially Equivalent

510(k) numberK834370

Submission

Device name
Mulhollan Arthroscopic Needle Carrier
Applicant
Acufex Microsurgical, Inc.
Mchenry, IL, US
Received
December 13, 1983
Decision date
February 27, 1984
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
LXH – Orthopedic Manual Surgical Instrument
Device class
Class I (low risk)
Regulation
21 CFR 888.4540
Specialty
Orthopedic

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Questions and answers

When was Mulhollan Arthroscopic Needle Carrier cleared by the FDA?

Mulhollan Arthroscopic Needle Carrier (K834370) received a 510(k) decision of Substantially Equivalent on February 27, 1984, 76 days after the submission was received.

What is the product code of K834370?

The FDA product code is LXH – Orthopedic Manual Surgical Instrument, a Class I (low risk) device regulated under 21 CFR 888.4540.