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FDA 510(k)

ACCESSORIES FOE ORTHOPEDIC SURGICAL PROCEDURES

K-Number: K950592 · 1995-06-01

ApplicantEare Consulting Service
Decision Date1995-06-01
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ACCESSORIES FOE ORTHOPEDIC SURGICAL PROCEDURES is the device name listed in this FDA 510(k) record. The listed applicant is Eare Consulting Service. It received FDA 510(k) clearance on 1995-06-01 under 510(k) number K950592. The device is classified under product code HRX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACCESSORIES FOE ORTHOPEDIC SURGICAL PROCEDURES?

ACCESSORIES FOE ORTHOPEDIC SURGICAL PROCEDURES is a medical device that received FDA 510(k) clearance on 1995-06-01. The listed applicant is Eare Consulting Service. The 510(k) number is K950592.

When did ACCESSORIES FOE ORTHOPEDIC SURGICAL PROCEDURES receive FDA 510(k) clearance?

ACCESSORIES FOE ORTHOPEDIC SURGICAL PROCEDURES received FDA 510(k) clearance on 1995-06-01, under 510(k) number K950592.

Who is the listed applicant for ACCESSORIES FOE ORTHOPEDIC SURGICAL PROCEDURES?

The FDA 510(k) record lists Eare Consulting Service as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ACCESSORIES FOE ORTHOPEDIC SURGICAL PROCEDURES?

The FDA product code for ACCESSORIES FOE ORTHOPEDIC SURGICAL PROCEDURES is HRX.

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Other records listing Eare Consulting Service as applicant

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K970180VSA 3000 VIBRATORYN SENSORY ANALYZERK944428LITE-BLADEK934981DENTAL DRILL

Related Devices (Code: HRX)

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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Official Source

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