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FDA 510(k)

TEST, MONO., DIFFERENTIAL SLIDE

K-Number: K760032 · 1976-08-03

ApplicantGamma Biologicals, Inc.
Decision Date1976-08-03
Product CodeKIN
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

TEST, MONO., DIFFERENTIAL SLIDE is the device name listed in this FDA 510(k) record. The listed applicant is Gamma Biologicals, Inc.. It received FDA 510(k) clearance on 1976-08-03 under 510(k) number K760032. The device is classified under product code KIN. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TEST, MONO., DIFFERENTIAL SLIDE?

TEST, MONO., DIFFERENTIAL SLIDE is a medical device that received FDA 510(k) clearance on 1976-08-03. The listed applicant is Gamma Biologicals, Inc.. The 510(k) number is K760032.

When did TEST, MONO., DIFFERENTIAL SLIDE receive FDA 510(k) clearance?

TEST, MONO., DIFFERENTIAL SLIDE received FDA 510(k) clearance on 1976-08-03, under 510(k) number K760032.

Who is the listed applicant for TEST, MONO., DIFFERENTIAL SLIDE?

The FDA 510(k) record lists Gamma Biologicals, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TEST, MONO., DIFFERENTIAL SLIDE?

The FDA product code for TEST, MONO., DIFFERENTIAL SLIDE is KIN.

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Other records listing Gamma Biologicals, 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.

K864207DISPOSABLE TEST CARDS/GAMMA SLIDE TEST INFECT MONOK861016GAMMA SLIDE TEST FOR INFECTIOUS MONONUCLEOSISK832473GAMMA SLIDE TEST FOR PREGNANCYK820647GAMMA FETAL BLEED SCREENING TESTK813342GAMMA CHLOROQUINE DIPHOSPHATE SOLUTIONK820072FE-CULT PLUS

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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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