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FDA 510(k)

BARRON TWIN BLADE TREPHINE FOR EPPIKARATOPHAKIA

K-Number: K860648 · 1986-03-25

ApplicantPrecision Instruments, Inc.
Decision Date1986-03-25
Product CodeHRH
Advisory CommitteeOP
DecisionSubstantially Equivalent for Some Indications

Device Summary

BARRON TWIN BLADE TREPHINE FOR EPPIKARATOPHAKIA 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 1986-03-25 under 510(k) number K860648. The device is classified under product code HRH. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the BARRON TWIN BLADE TREPHINE FOR EPPIKARATOPHAKIA?

BARRON TWIN BLADE TREPHINE FOR EPPIKARATOPHAKIA is a medical device that received FDA 510(k) clearance on 1986-03-25. The listed applicant is Precision Instruments, Inc.. The 510(k) number is K860648.

When did BARRON TWIN BLADE TREPHINE FOR EPPIKARATOPHAKIA receive FDA 510(k) clearance?

BARRON TWIN BLADE TREPHINE FOR EPPIKARATOPHAKIA received FDA 510(k) clearance on 1986-03-25, under 510(k) number K860648.

Who is the listed applicant for BARRON TWIN BLADE TREPHINE FOR EPPIKARATOPHAKIA?

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 TWIN BLADE TREPHINE FOR EPPIKARATOPHAKIA?

The FDA product code for BARRON TWIN BLADE TREPHINE FOR EPPIKARATOPHAKIA is HRH.

Related Clinical Trials

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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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.

K864520BARRON ROTARY BLADE TREPHINE USING HESSBURG-BARRONK843048RING 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.K864520BARRON ROTARY BLADE TREPHINE USING HESSBURG-BARRONPrecision Instruments, Inc.K862524DEKNATEL (R) TREPHINEDeknatel, Inc.K861825CORNEAL TRANSPLANT TREPHINE DISPOSABLE BLADEStorz Instrument Co.

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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