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FDA 510(k)

OBSTETRICAL SAFETY SYSTEM

K-Number: K884868 · 1989-03-01

ApplicantBuckman Co., Inc.
Decision Date1989-03-01
Product CodeKNC
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

OBSTETRICAL SAFETY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Buckman Co., Inc.. It received FDA 510(k) clearance on 1989-03-01 under 510(k) number K884868. The device is classified under product code KNC. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OBSTETRICAL SAFETY SYSTEM?

OBSTETRICAL SAFETY SYSTEM is a medical device that received FDA 510(k) clearance on 1989-03-01. The listed applicant is Buckman Co., Inc.. The 510(k) number is K884868.

When did OBSTETRICAL SAFETY SYSTEM receive FDA 510(k) clearance?

OBSTETRICAL SAFETY SYSTEM received FDA 510(k) clearance on 1989-03-01, under 510(k) number K884868.

Who is the listed applicant for OBSTETRICAL SAFETY SYSTEM?

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

What is the FDA product code for OBSTETRICAL SAFETY SYSTEM?

The FDA product code for OBSTETRICAL SAFETY SYSTEM is KNC.

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Other records listing Buckman Co., Inc. as applicant

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Related Devices (Code: KNC)

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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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