In-Sight Surgical Instrument Kits, Disposable

FDA 510(k) K910816 · Insight International, Inc.

Unknown

510(k) numberK910816

Submission

Device name
In-Sight Surgical Instrument Kits, Disposable
Applicant
Insight International, Inc.
Pawtucket, RI, US
Received
February 26, 1991
Decision date
April 17, 1991
Decision
Unknown (SESK)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
KDD – Kit, Surgical Instrument, Disposable
Device class
Class I (low risk)
Regulation
21 CFR 878.4800
Specialty
General, Plastic Surgery

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K960456Denver Paracentesis NEEDLE(60-1200) Denver Paracentesis Needle with Drainage…KDD · Traditional Denver Biomaterials, Inc.04/01/1996SE
K936255Custom CV PackKDD · Traditional Associated Medical03/31/1994SN
K932219Suture Set or Laceration Trays (Packs)KDD · Traditional Associated Medical Products Co.07/09/1993SESK
K923176Surgical Instrument Kit, DisposableKDD · Traditional Ulti-Med Intl., Inc.06/17/1993SE
K925905Kit, Surgical Instrument, DisposableKDD · Traditional Kay Medical Concepts06/16/1993SESK
K924958Biopsy/Myelo/Arthro/Amniocent/Basic Skin Prep TrayKDD · Traditional Medical Insights, Inc.06/07/1993SEKD
K925215Sterile Surgical Instrument TraysKDD · Traditional American Healthcare Supply Co., Inc.06/01/1993SEKD

More from American Healthcare Supply Co., Inc.

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Questions and answers

When was In-Sight Surgical Instrument Kits, Disposable cleared by the FDA?

In-Sight Surgical Instrument Kits, Disposable (K910816) received a 510(k) decision of Unknown on April 17, 1991, 50 days after the submission was received.

What is the product code of K910816?

The FDA product code is KDD – Kit, Surgical Instrument, Disposable, a Class I (low risk) device regulated under 21 CFR 878.4800.