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FDA 510(k)

KINGS BAY PRELUDE ONE STEP HCG COMBO KIT

K-Number: K931698 · 1993-11-05

Decision Date1993-11-05
Product CodeJHI
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

KINGS BAY PRELUDE ONE STEP HCG COMBO KIT is the device name listed in this FDA 510(k) record. The listed applicant is King'S Bay Intl., Inc.. It received FDA 510(k) clearance on 1993-11-05 under 510(k) number K931698. 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 KINGS BAY PRELUDE ONE STEP HCG COMBO KIT?

KINGS BAY PRELUDE ONE STEP HCG COMBO KIT is a medical device that received FDA 510(k) clearance on 1993-11-05. The listed applicant is King'S Bay Intl., Inc.. The 510(k) number is K931698.

When did KINGS BAY PRELUDE ONE STEP HCG COMBO KIT receive FDA 510(k) clearance?

KINGS BAY PRELUDE ONE STEP HCG COMBO KIT received FDA 510(k) clearance on 1993-11-05, under 510(k) number K931698.

Who is the listed applicant for KINGS BAY PRELUDE ONE STEP HCG COMBO KIT?

The FDA 510(k) record lists King'S Bay Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KINGS BAY PRELUDE ONE STEP HCG COMBO KIT?

The FDA product code for KINGS BAY PRELUDE ONE STEP HCG COMBO KIT 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.

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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