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FDA 510(k)

ABDOMINAL SPATULA

K-Number: K890374 · 1989-02-03

ApplicantKinetic Medical Products
Decision Date1989-02-03
Product CodeGAF
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ABDOMINAL SPATULA 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 K890374. The device is classified under product code GAF. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ABDOMINAL SPATULA?

ABDOMINAL SPATULA 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 K890374.

When did ABDOMINAL SPATULA receive FDA 510(k) clearance?

ABDOMINAL SPATULA received FDA 510(k) clearance on 1989-02-03, under 510(k) number K890374.

Who is the listed applicant for ABDOMINAL SPATULA?

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 ABDOMINAL SPATULA?

The FDA product code for ABDOMINAL SPATULA is GAF.

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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 FORCEPSK890387MALLEABLE PLACENTA CURETTEK890380CERVICAL BIOPSY FORCEPSK890376VAGINAL SPECULUMK890382COMPRESSION FORCEPSK890383HYSTERECTOMY FORCEPS

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Related Devices (Code: GAF)

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.

K023688LEMAITRE VASCULAR DISPOSABLE VEIN STRIPPERLeMaitre Vascular, Inc.K935357SNAP RECIPROCATING SAWSurgiquip, Inc.K882793PMT FUKUSHIMA MICROSURGICAL INSTRUMENT LINEPmt Corp.K822108CEMENT-PICKBio-Blitz, 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.

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