Disposable Hemostats

FDA 510(k) K920298 · Falcon Instruments, Inc.

Substantially Equivalent

510(k) numberK920298

Submission

Device name
Disposable Hemostats
Applicant
Falcon Instruments, Inc.
Bethesda, MD, US
Received
January 22, 1992
Decision date
August 11, 1992
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
HRQ – Hemostat
Device class
Class I (low risk)
Regulation
21 CFR 878.4800
Specialty
General, Plastic Surgery

Other 510(k)s with product code HRQ

510(k)DeviceApplicantDecision
K895683Bernard Vessel ApproximatorHRQ · Traditional Applied Medical Technologies10/24/1989SE
K890245Surgical HemostatsHRQ · Traditional Kinetic Medical Products01/27/1989SE
K884196Surgical Instruments (Various Types & Sizes)HRQ · Traditional Disposable Sterile Surgical Instruments, Inc.11/08/1988SE
K881937Surgical InstrumentsHRQ · Traditional Far East Intl. Trading Corp.06/15/1988SE
K861807Medcare Hemostats (Straight, Curved, Mosquito-Tip)HRQ · Traditional Medcomp Technologies, Inc.05/23/1986SE
K844152HemstatsHRQ · Traditional I M, Inc.11/07/1984SE
K843593Surgipress Surgical LoopHRQ · Traditional Syntex Corp.10/24/1984SE
K841514Scanlan Vascu-Statt II ApproximatorHRQ · Traditional Scanlan Intl., Inc.06/05/1984SE
K834175Op-Con Surg. Instruments #11HRQ · Traditional Imm Enterprises , Ltd.01/27/1984SE
K831797HemostatsHRQ · Traditional I M, Inc.07/19/1983SE

More from I M, Inc.

510(k)DeviceDecision
K930775Disposable Forceps, Hemostats, Needle Guides, EtcMDM · Traditional 04/23/1993SE
K920297Disposable ScissorsMDM · Traditional 09/11/1992SE
K920296Disposable ForcepsMDM · Traditional 09/11/1992SE

Questions and answers

When was Disposable Hemostats cleared by the FDA?

Disposable Hemostats (K920298) received a 510(k) decision of Substantially Equivalent on August 11, 1992, 202 days after the submission was received.

What is the product code of K920298?

The FDA product code is HRQ – Hemostat, a Class I (low risk) device regulated under 21 CFR 878.4800.