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FDA 510(k)

RIANEN FOLLICLE STIMULATING HORMONE

K-Number: K834038 · 1984-01-30

ApplicantNew England Nuclear
Decision Date1984-01-30
Product CodeCGJ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

RIANEN FOLLICLE STIMULATING HORMONE is the device name listed in this FDA 510(k) record. The listed applicant is New England Nuclear. It received FDA 510(k) clearance on 1984-01-30 under 510(k) number K834038. The device is classified under product code CGJ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RIANEN FOLLICLE STIMULATING HORMONE?

RIANEN FOLLICLE STIMULATING HORMONE is a medical device that received FDA 510(k) clearance on 1984-01-30. The listed applicant is New England Nuclear. The 510(k) number is K834038.

When did RIANEN FOLLICLE STIMULATING HORMONE receive FDA 510(k) clearance?

RIANEN FOLLICLE STIMULATING HORMONE received FDA 510(k) clearance on 1984-01-30, under 510(k) number K834038.

Who is the listed applicant for RIANEN FOLLICLE STIMULATING HORMONE?

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

What is the FDA product code for RIANEN FOLLICLE STIMULATING HORMONE?

The FDA product code for RIANEN FOLLICLE STIMULATING HORMONE is CGJ.

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Other records listing New England Nuclear as applicant

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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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