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FDA 510(k)

MIDWIFERY/OBSTETRICAL FORCEPS

K-Number: K890385 · 1989-03-01

ApplicantKinetic Medical Products
Decision Date1989-03-01
Product CodeHDA
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

MIDWIFERY/OBSTETRICAL FORCEPS 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 1989-03-01 under 510(k) number K890385. The device is classified under product code HDA. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MIDWIFERY/OBSTETRICAL FORCEPS?

MIDWIFERY/OBSTETRICAL FORCEPS is a medical device that received FDA 510(k) clearance on 1989-03-01. The listed applicant is Kinetic Medical Products. The 510(k) number is K890385.

When did MIDWIFERY/OBSTETRICAL FORCEPS receive FDA 510(k) clearance?

MIDWIFERY/OBSTETRICAL FORCEPS received FDA 510(k) clearance on 1989-03-01, under 510(k) number K890385.

Who is the listed applicant for MIDWIFERY/OBSTETRICAL FORCEPS?

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 MIDWIFERY/OBSTETRICAL FORCEPS?

The FDA product code for MIDWIFERY/OBSTETRICAL FORCEPS is HDA.

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Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Other records listing Kinetic Medical Products as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K890380CERVICAL BIOPSY FORCEPSK890387MALLEABLE PLACENTA CURETTEK890382COMPRESSION FORCEPSK890376VAGINAL SPECULUMK890216MICROSURGICAL KERATOMEK890383HYSTERECTOMY FORCEPS

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Related Devices (Code: HDA)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K100517INSTRUMED FORCEPS OBSTERICAL, MODEL# 46-5XXX, OB-XXXXInstrumed International, Inc.K092827DIMELA OBSTERICAL FORCEPS, MODEL 72.1 XX XXDimeda Instrumente GmbHK013747TEKNO-MEDICAL OBSTETRICAL FORCEPSTekno Medical Optik-Chirurgie GmbH & Co.K951529V. MUELLER OBSTETRICAL (OB) FORCEPSBaxter Healthcare CorpK914552CMI VACUUM PUMPColumbia Medical & Surgical, Inc.K905583ILC FORCEPS PADSInman Liebelt Corp.

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.

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