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FDA 510(k)

FETAL BLOOD SAMPLING KIT MODEL 1560

K-Number: K810028 · 1981-01-16

Decision Date1981-01-16
Product CodeHGW
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

FETAL BLOOD SAMPLING KIT MODEL 1560 is the device name listed in this FDA 510(k) record. The listed applicant is Transidyne General Corp.. It received FDA 510(k) clearance on 1981-01-16 under 510(k) number K810028. The device is classified under product code HGW. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FETAL BLOOD SAMPLING KIT MODEL 1560?

FETAL BLOOD SAMPLING KIT MODEL 1560 is a medical device that received FDA 510(k) clearance on 1981-01-16. The listed applicant is Transidyne General Corp.. The 510(k) number is K810028.

When did FETAL BLOOD SAMPLING KIT MODEL 1560 receive FDA 510(k) clearance?

FETAL BLOOD SAMPLING KIT MODEL 1560 received FDA 510(k) clearance on 1981-01-16, under 510(k) number K810028.

Who is the listed applicant for FETAL BLOOD SAMPLING KIT MODEL 1560?

The FDA 510(k) record lists Transidyne General Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FETAL BLOOD SAMPLING KIT MODEL 1560?

The FDA product code for FETAL BLOOD SAMPLING KIT MODEL 1560 is HGW.

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 Transidyne General Corp. 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 21 devices →

Related Devices (Code: HGW)

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.

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