Safety Pins & Rubber Bands

FDA 510(k) K831915 · Ormed Mfg., Inc.

Substantially Equivalent

510(k) numberK831915

Submission

Device name
Safety Pins & Rubber Bands
Applicant
Ormed Mfg., Inc.
Mchenry, IL, US
Received
June 14, 1983
Decision date
September 12, 1983
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

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

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K920153Thermuff BagKDC · Traditional Techstyles07/01/1992SE
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K905240VesseloopsKDC · Traditional Sparta Surgical Corp.02/06/1991SE
K903649Bradley Tenaculum HolderKDC · Traditional Marlo Surgical Technology11/02/1990SE

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K880911Blunt SpongeEFQ · Traditional 03/17/1988SE
K880910Round Stick SpongesEFQ · Traditional 03/17/1988SE
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K880854Strung Absorbent BallsEFQ · Traditional 03/17/1988SE

Questions and answers

When was Safety Pins & Rubber Bands cleared by the FDA?

Safety Pins & Rubber Bands (K831915) received a 510(k) decision of Substantially Equivalent on September 12, 1983, 90 days after the submission was received.

What is the product code of K831915?

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