FDA 510(k)

INTESTINAL CRUSHING CLAMP

K-Number: K890371 · 1989-02-03

Decision Date1989-02-03

Product CodeHXD

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

INTESTINAL CRUSHING CLAMP is the device name listed in this FDA 510(k) record. The listed applicant is Kinetic Medical Products. It received FDA 510(k) clearance on 1989-02-03 under 510(k) number K890371. The device is classified under product code HXD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTESTINAL CRUSHING CLAMP?

INTESTINAL CRUSHING CLAMP is a medical device that received FDA 510(k) clearance on 1989-02-03. The listed applicant is Kinetic Medical Products. The 510(k) number is K890371.

When did INTESTINAL CRUSHING CLAMP receive FDA 510(k) clearance?

INTESTINAL CRUSHING CLAMP received FDA 510(k) clearance on 1989-02-03, under 510(k) number K890371.

Who is the listed applicant for INTESTINAL CRUSHING CLAMP?

The FDA 510(k) record lists Kinetic Medical Products as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INTESTINAL CRUSHING CLAMP?

The FDA product code for INTESTINAL CRUSHING CLAMP is HXD.

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Other records listing Kinetic Medical Products as applicant

K890385MIDWIFERY/OBSTETRICAL FORCEPS K890380CERVICAL BIOPSY FORCEPS K890387MALLEABLE PLACENTA CURETTE K890382COMPRESSION FORCEPS K890376VAGINAL SPECULUM K890383HYSTERECTOMY FORCEPS

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Related Devices (Code: HXD)

K890372INTESTINAL CLAMPKinetic Medical Products K890381PARAMETRIUM CLAMPKinetic Medical Products K890368KIDNEY CLAMPKinetic Medical Products K874959VASCULAR CLAMPSolway, Inc.K872386C CLAMPMed-Tool, Inc.K863653SUCTION-OFFB&B Medical 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.