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FDA 510(k)

BARRON ROTARY BLADE TREPHINE USING HESSBURG-BARRON

K-Number: K864520 · 1987-01-20

ApplicantPrecision Instruments, Inc.
Decision Date1987-01-20
Product CodeHRH
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

BARRON ROTARY BLADE TREPHINE USING HESSBURG-BARRON is the device name listed in this FDA 510(k) record. The listed applicant is Precision Instruments, Inc.. It received FDA 510(k) clearance on 1987-01-20 under 510(k) number K864520. The device is classified under product code HRH. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BARRON ROTARY BLADE TREPHINE USING HESSBURG-BARRON?

BARRON ROTARY BLADE TREPHINE USING HESSBURG-BARRON is a medical device that received FDA 510(k) clearance on 1987-01-20. The listed applicant is Precision Instruments, Inc.. The 510(k) number is K864520.

When did BARRON ROTARY BLADE TREPHINE USING HESSBURG-BARRON receive FDA 510(k) clearance?

BARRON ROTARY BLADE TREPHINE USING HESSBURG-BARRON received FDA 510(k) clearance on 1987-01-20, under 510(k) number K864520.

Who is the listed applicant for BARRON ROTARY BLADE TREPHINE USING HESSBURG-BARRON?

The FDA 510(k) record lists Precision Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BARRON ROTARY BLADE TREPHINE USING HESSBURG-BARRON?

The FDA product code for BARRON ROTARY BLADE TREPHINE USING HESSBURG-BARRON is HRH.

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Other records listing Precision Instruments, Inc. 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.

K860648BARRON TWIN BLADE TREPHINE FOR EPPIKARATOPHAKIAK843048RING SUPPORTED TREPHINE FOR CORNEA TRANSK801585HESSBURG-BFRRON TREPHINE

Related Devices (Code: HRH)

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.

K022843GAYHEART CORNEAL EXCISION DEVICEStephens InstrumentsK931792ARTHROSCOPEIntramed Laboratories, Inc.K873918HEAD & CHIN RESTSRichmond Products, Inc.K862524DEKNATEL (R) TREPHINEDeknatel, Inc.K861825CORNEAL TRANSPLANT TREPHINE DISPOSABLE BLADEStorz Instrument Co.K860648BARRON TWIN BLADE TREPHINE FOR EPPIKARATOPHAKIAPrecision Instruments, 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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