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FDA 510(k)

DR.BRUNO LANGE MINI-HBA1 PHOTOMETER

K-Number: K865055 · 1987-03-19

ApplicantDiversa Corp.
Decision Date1987-03-19
Product CodeGKR
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

DR.BRUNO LANGE MINI-HBA1 PHOTOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Diversa Corp.. It received FDA 510(k) clearance on 1987-03-19 under 510(k) number K865055. The device is classified under product code GKR. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DR.BRUNO LANGE MINI-HBA1 PHOTOMETER?

DR.BRUNO LANGE MINI-HBA1 PHOTOMETER is a medical device that received FDA 510(k) clearance on 1987-03-19. The listed applicant is Diversa Corp.. The 510(k) number is K865055.

When did DR.BRUNO LANGE MINI-HBA1 PHOTOMETER receive FDA 510(k) clearance?

DR.BRUNO LANGE MINI-HBA1 PHOTOMETER received FDA 510(k) clearance on 1987-03-19, under 510(k) number K865055.

Who is the listed applicant for DR.BRUNO LANGE MINI-HBA1 PHOTOMETER?

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

What is the FDA product code for DR.BRUNO LANGE MINI-HBA1 PHOTOMETER?

The FDA product code for DR.BRUNO LANGE MINI-HBA1 PHOTOMETER is GKR.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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