FDA 510(k)

GENDER CHOICE INFORMATION KIT, FEMALE AND MALE

K-Number: K870999 · 1987-07-14

ApplicantProcare C/O Wiley, Rein & Fielding

Decision Date1987-07-14

Product CodeLHD

DecisionSubstantially Equivalent

Device Summary

GENDER CHOICE INFORMATION KIT, FEMALE AND MALE is the device name listed in this FDA 510(k) record. The listed applicant is Procare C/O Wiley, Rein & Fielding. It received FDA 510(k) clearance on 1987-07-14 under 510(k) number K870999. The device is classified under product code LHD. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GENDER CHOICE INFORMATION KIT, FEMALE AND MALE?

GENDER CHOICE INFORMATION KIT, FEMALE AND MALE is a medical device that received FDA 510(k) clearance on 1987-07-14. The listed applicant is Procare C/O Wiley, Rein & Fielding. The 510(k) number is K870999.

When did GENDER CHOICE INFORMATION KIT, FEMALE AND MALE receive FDA 510(k) clearance?

GENDER CHOICE INFORMATION KIT, FEMALE AND MALE received FDA 510(k) clearance on 1987-07-14, under 510(k) number K870999.

Who is the listed applicant for GENDER CHOICE INFORMATION KIT, FEMALE AND MALE?

The FDA 510(k) record lists Procare C/O Wiley, Rein & Fielding as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GENDER CHOICE INFORMATION KIT, FEMALE AND MALE?

The FDA product code for GENDER CHOICE INFORMATION KIT, FEMALE AND MALE is LHD.

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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.