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FDA 510(k)

BIO-RAD BLIND PERFOR. SPECIMEN SET FOR NIDA REG.

K-Number: K895816 · 1989-12-07

ApplicantBio-Rad
Decision Date1989-12-07
Product CodeDIF
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

BIO-RAD BLIND PERFOR. SPECIMEN SET FOR NIDA REG. is the device name listed in this FDA 510(k) record. The listed applicant is Bio-Rad. It received FDA 510(k) clearance on 1989-12-07 under 510(k) number K895816. The device is classified under product code DIF. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BIO-RAD BLIND PERFOR. SPECIMEN SET FOR NIDA REG.?

BIO-RAD BLIND PERFOR. SPECIMEN SET FOR NIDA REG. is a medical device that received FDA 510(k) clearance on 1989-12-07. The listed applicant is Bio-Rad. The 510(k) number is K895816.

When did BIO-RAD BLIND PERFOR. SPECIMEN SET FOR NIDA REG. receive FDA 510(k) clearance?

BIO-RAD BLIND PERFOR. SPECIMEN SET FOR NIDA REG. received FDA 510(k) clearance on 1989-12-07, under 510(k) number K895816.

Who is the listed applicant for BIO-RAD BLIND PERFOR. SPECIMEN SET FOR NIDA REG.?

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 BIO-RAD BLIND PERFOR. SPECIMEN SET FOR NIDA REG.?

The FDA product code for BIO-RAD BLIND PERFOR. SPECIMEN SET FOR NIDA REG. is DIF.

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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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