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FDA 510(k)

SURGICAL PROBE

K-Number: K890227 · 1989-01-27

ApplicantKinetic Medical Products
Decision Date1989-01-27
Product CodeHXB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SURGICAL PROBE 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 1989-01-27 under 510(k) number K890227. The device is classified under product code HXB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SURGICAL PROBE?

SURGICAL PROBE is a medical device that received FDA 510(k) clearance on 1989-01-27. The listed applicant is Kinetic Medical Products. The 510(k) number is K890227.

When did SURGICAL PROBE receive FDA 510(k) clearance?

SURGICAL PROBE received FDA 510(k) clearance on 1989-01-27, under 510(k) number K890227.

Who is the listed applicant for SURGICAL PROBE?

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 SURGICAL PROBE?

The FDA product code for SURGICAL PROBE is HXB.

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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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Related Devices (Code: HXB)

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.

K960539DIAO HAND SURGERY SETKinetikos Medical, Inc.K943472COHORT AVB RETRACTOR SYSTEMCohort Medical Products Group, Inc.K912843FLEXMEDICS RETRACT ORTH PROBE, PETTINE BONE PROBEFlexmedicsK873652HOOK PROBE #TM-1376Arthropedics, Inc.K873651BLUNT MEASURING PROBE W/2MM GRADATIONS #TM-1375Arthropedics, Inc.K863149BOWEN PROBEBowen & Company, 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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