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FDA 510(k)

BIOCHRON FERTILITY INDICATOR

K-Number: K852801 · 1985-09-19

ApplicantFertil-A-Chron, Inc.
Decision Date1985-09-19
Product CodeLHD
DecisionSubstantially Equivalent

Device Summary

BIOCHRON FERTILITY INDICATOR is the device name listed in this FDA 510(k) record. The listed applicant is Fertil-A-Chron, Inc.. It received FDA 510(k) clearance on 1985-09-19 under 510(k) number K852801. The device is classified under product code LHD. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BIOCHRON FERTILITY INDICATOR?

BIOCHRON FERTILITY INDICATOR is a medical device that received FDA 510(k) clearance on 1985-09-19. The listed applicant is Fertil-A-Chron, Inc.. The 510(k) number is K852801.

When did BIOCHRON FERTILITY INDICATOR receive FDA 510(k) clearance?

BIOCHRON FERTILITY INDICATOR received FDA 510(k) clearance on 1985-09-19, under 510(k) number K852801.

Who is the listed applicant for BIOCHRON FERTILITY INDICATOR?

The FDA 510(k) record lists Fertil-A-Chron, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BIOCHRON FERTILITY INDICATOR?

The FDA product code for BIOCHRON FERTILITY INDICATOR 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.

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