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)

WARD'S BREAST MEASURING DEVICE

K-Number: K870887 · 1987-03-31

Decision Date1987-03-31
Product Code
DecisionSubstantially Equivalent

Device Summary

WARD'S BREAST MEASURING DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Downs Surgical , Ltd.. It received FDA 510(k) clearance on 1987-03-31 under 510(k) number K870887. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WARD'S BREAST MEASURING DEVICE?

WARD'S BREAST MEASURING DEVICE is a medical device that received FDA 510(k) clearance on 1987-03-31. The listed applicant is Downs Surgical , Ltd.. The 510(k) number is K870887.

When did WARD'S BREAST MEASURING DEVICE receive FDA 510(k) clearance?

WARD'S BREAST MEASURING DEVICE received FDA 510(k) clearance on 1987-03-31, under 510(k) number K870887.

Who is the listed applicant for WARD'S BREAST MEASURING DEVICE?

The FDA 510(k) record lists Downs Surgical , Ltd. as the applicant. This does not by itself establish the device manufacturer.

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 Downs Surgical , Ltd. 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 60 devices →

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.

↑