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FDA 510(k)

ACCUPOINT HCG PREGNANCY TEST AND ACCESSORIES

K-Number: K872130 · 1987-07-16

ApplicantSyva Co.
Decision Date1987-07-16
Product CodeJHI
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ACCUPOINT HCG PREGNANCY TEST AND ACCESSORIES is the device name listed in this FDA 510(k) record. The listed applicant is Syva Co.. It received FDA 510(k) clearance on 1987-07-16 under 510(k) number K872130. The device is classified under product code JHI. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACCUPOINT HCG PREGNANCY TEST AND ACCESSORIES?

ACCUPOINT HCG PREGNANCY TEST AND ACCESSORIES is a medical device that received FDA 510(k) clearance on 1987-07-16. The listed applicant is Syva Co.. The 510(k) number is K872130.

When did ACCUPOINT HCG PREGNANCY TEST AND ACCESSORIES receive FDA 510(k) clearance?

ACCUPOINT HCG PREGNANCY TEST AND ACCESSORIES received FDA 510(k) clearance on 1987-07-16, under 510(k) number K872130.

Who is the listed applicant for ACCUPOINT HCG PREGNANCY TEST AND ACCESSORIES?

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

What is the FDA product code for ACCUPOINT HCG PREGNANCY TEST AND ACCESSORIES?

The FDA product code for ACCUPOINT HCG PREGNANCY TEST AND ACCESSORIES is JHI.

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 Syva Co. 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 448 devices →

Related Devices (Code: JHI)

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

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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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