Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

SAS ONE-STEP PREGNANCY

K-Number: K990741 · 1999-05-10

Decision Date1999-05-10
Product CodeJHI
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

SAS ONE-STEP PREGNANCY is the device name listed in this FDA 510(k) record. The listed applicant is Sa Scientific, Inc.. It received FDA 510(k) clearance on 1999-05-10 under 510(k) number K990741. 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 SAS ONE-STEP PREGNANCY?

SAS ONE-STEP PREGNANCY is a medical device that received FDA 510(k) clearance on 1999-05-10. The listed applicant is Sa Scientific, Inc.. The 510(k) number is K990741.

When did SAS ONE-STEP PREGNANCY receive FDA 510(k) clearance?

SAS ONE-STEP PREGNANCY received FDA 510(k) clearance on 1999-05-10, under 510(k) number K990741.

Who is the listed applicant for SAS ONE-STEP PREGNANCY?

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

What is the FDA product code for SAS ONE-STEP PREGNANCY?

The FDA product code for SAS ONE-STEP PREGNANCY 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 Sa Scientific, 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.

View all 199 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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑