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FDA 510(k)

MEDICAL LABS FETAL SCAN #1000 W/CENTRAL

K-Number: K822830 · 1982-09-30

ApplicantCranbury Medical Labs, Inc.
Decision Date1982-09-30
Product CodeHGM
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

MEDICAL LABS FETAL SCAN #1000 W/CENTRAL is the device name listed in this FDA 510(k) record. The listed applicant is Cranbury Medical Labs, Inc.. It received FDA 510(k) clearance on 1982-09-30 under 510(k) number K822830. The device is classified under product code HGM. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDICAL LABS FETAL SCAN #1000 W/CENTRAL?

MEDICAL LABS FETAL SCAN #1000 W/CENTRAL is a medical device that received FDA 510(k) clearance on 1982-09-30. The listed applicant is Cranbury Medical Labs, Inc.. The 510(k) number is K822830.

When did MEDICAL LABS FETAL SCAN #1000 W/CENTRAL receive FDA 510(k) clearance?

MEDICAL LABS FETAL SCAN #1000 W/CENTRAL received FDA 510(k) clearance on 1982-09-30, under 510(k) number K822830.

Who is the listed applicant for MEDICAL LABS FETAL SCAN #1000 W/CENTRAL?

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

What is the FDA product code for MEDICAL LABS FETAL SCAN #1000 W/CENTRAL?

The FDA product code for MEDICAL LABS FETAL SCAN #1000 W/CENTRAL is HGM.

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Other records listing Cranbury Medical Labs, Inc. as applicant

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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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