EARLY PREGNANCY DETECTION
K-Number: K811398 · 1981-05-29
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Device Summary
Frequently Asked Questions
What is the EARLY PREGNANCY DETECTION?
EARLY PREGNANCY DETECTION is a medical device that received FDA 510(k) clearance on 1981-05-29. The listed applicant is Immuchem Corp.. The 510(k) number is K811398.
When did EARLY PREGNANCY DETECTION receive FDA 510(k) clearance?
EARLY PREGNANCY DETECTION received FDA 510(k) clearance on 1981-05-29, under 510(k) number K811398.
Who is the listed applicant for EARLY PREGNANCY DETECTION?
The FDA 510(k) record lists Immuchem Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EARLY PREGNANCY DETECTION?
The FDA product code for EARLY PREGNANCY DETECTION 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 Immuchem Corp. 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.
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
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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