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FDA 510(k)

DIGILAB CAMBRIDGE PERIMETER

K-Number: K860115 · 1986-02-27

ApplicantBio-Rad
Decision Date1986-02-27
Product CodeHOO
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

DIGILAB CAMBRIDGE PERIMETER is the device name listed in this FDA 510(k) record. The listed applicant is Bio-Rad. It received FDA 510(k) clearance on 1986-02-27 under 510(k) number K860115. The device is classified under product code HOO. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIGILAB CAMBRIDGE PERIMETER?

DIGILAB CAMBRIDGE PERIMETER is a medical device that received FDA 510(k) clearance on 1986-02-27. The listed applicant is Bio-Rad. The 510(k) number is K860115.

When did DIGILAB CAMBRIDGE PERIMETER receive FDA 510(k) clearance?

DIGILAB CAMBRIDGE PERIMETER received FDA 510(k) clearance on 1986-02-27, under 510(k) number K860115.

Who is the listed applicant for DIGILAB CAMBRIDGE PERIMETER?

The FDA 510(k) record lists Bio-Rad as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DIGILAB CAMBRIDGE PERIMETER?

The FDA product code for DIGILAB CAMBRIDGE PERIMETER is HOO.

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Other records listing Bio-Rad 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.

K171061MRSASelect IIK122187VRESELECT CULTURE MEDIUMK103684VRESELECT CULTURE MEDIUMK093678PLATELIA ASPERGILLUS EIA MODEL 62793K100589MRSA SELECT - SKIN AND SOFT TISSUE WOUND SPECIMENSK081362PLATELIA LYME IGM

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Related Devices (Code: HOO)

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.

K941723WELCH ALLYN GLAUCOMA DETECTORWelch Allyn, Inc.K930448MARCO PROJECTION PERIMETERMarco Ophthalmic, Inc.K873912RICHMOND VISUAL FIELD SCREENERRichmond Products, Inc.K864467HENSON - HAMBLIN CFS 2000 CENTRAL FIELD SCREENKeeler Instruments, Inc.K832800AUTOMATIC TANGENT SCREEN 50CooperVision, 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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