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FDA 510(k)

CEPHALOTOMY SCISSORS

K-Number: K890388 · 1989-02-13

ApplicantKinetic Medical Products
Decision Date1989-02-13
Product CodeKNB
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

CEPHALOTOMY SCISSORS 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 1989-02-13 under 510(k) number K890388. The device is classified under product code KNB. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CEPHALOTOMY SCISSORS?

CEPHALOTOMY SCISSORS is a medical device that received FDA 510(k) clearance on 1989-02-13. The listed applicant is Kinetic Medical Products. The 510(k) number is K890388.

When did CEPHALOTOMY SCISSORS receive FDA 510(k) clearance?

CEPHALOTOMY SCISSORS received FDA 510(k) clearance on 1989-02-13, under 510(k) number K890388.

Who is the listed applicant for CEPHALOTOMY SCISSORS?

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 CEPHALOTOMY SCISSORS?

The FDA product code for CEPHALOTOMY SCISSORS is KNB.

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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.

K890385MIDWIFERY/OBSTETRICAL FORCEPSK890380CERVICAL BIOPSY FORCEPSK890387MALLEABLE PLACENTA CURETTEK890382COMPRESSION FORCEPSK890376VAGINAL SPECULUMK890383HYSTERECTOMY FORCEPS

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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