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FDA 510(k)

PERINATAL COMPUTERS 2015/2025/2040/2045/2080/2085

K-Number: K870692 · 1987-05-04

Decision Date1987-05-04
Product CodeHGM
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

PERINATAL COMPUTERS 2015/2025/2040/2045/2080/2085 is the device name listed in this FDA 510(k) record. The listed applicant is Peritronics Research and Development, Inc.. It received FDA 510(k) clearance on 1987-05-04 under 510(k) number K870692. 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 PERINATAL COMPUTERS 2015/2025/2040/2045/2080/2085?

PERINATAL COMPUTERS 2015/2025/2040/2045/2080/2085 is a medical device that received FDA 510(k) clearance on 1987-05-04. The listed applicant is Peritronics Research and Development, Inc.. The 510(k) number is K870692.

When did PERINATAL COMPUTERS 2015/2025/2040/2045/2080/2085 receive FDA 510(k) clearance?

PERINATAL COMPUTERS 2015/2025/2040/2045/2080/2085 received FDA 510(k) clearance on 1987-05-04, under 510(k) number K870692.

Who is the listed applicant for PERINATAL COMPUTERS 2015/2025/2040/2045/2080/2085?

The FDA 510(k) record lists Peritronics Research and Development, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PERINATAL COMPUTERS 2015/2025/2040/2045/2080/2085?

The FDA product code for PERINATAL COMPUTERS 2015/2025/2040/2045/2080/2085 is HGM.

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 Peritronics Research and Development, Inc. 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.

Related Devices (Code: HGM)

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

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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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