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FDA 510(k)

DIGILAB MODEL 1500 PERIMETER

K-Number: K870120 · 1987-02-20

ApplicantBio-Rad
Decision Date1987-02-20
Product CodeHPT
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

DIGILAB MODEL 1500 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 1987-02-20 under 510(k) number K870120. The device is classified under product code HPT. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIGILAB MODEL 1500 PERIMETER?

DIGILAB MODEL 1500 PERIMETER is a medical device that received FDA 510(k) clearance on 1987-02-20. The listed applicant is Bio-Rad. The 510(k) number is K870120.

When did DIGILAB MODEL 1500 PERIMETER receive FDA 510(k) clearance?

DIGILAB MODEL 1500 PERIMETER received FDA 510(k) clearance on 1987-02-20, under 510(k) number K870120.

Who is the listed applicant for DIGILAB MODEL 1500 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 MODEL 1500 PERIMETER?

The FDA product code for DIGILAB MODEL 1500 PERIMETER is HPT.

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.

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.

View all 319 devices →

Related Devices (Code: HPT)

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.

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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