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FDA 510(k)

SONICAID TEAM

K-Number: K912639 · 1991-12-31

ApplicantOxford Medilog, Inc.
Decision Date1991-12-31
Product CodeHGM
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

SONICAID TEAM is the device name listed in this FDA 510(k) record. The listed applicant is Oxford Medilog, Inc.. It received FDA 510(k) clearance on 1991-12-31 under 510(k) number K912639. 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 SONICAID TEAM?

SONICAID TEAM is a medical device that received FDA 510(k) clearance on 1991-12-31. The listed applicant is Oxford Medilog, Inc.. The 510(k) number is K912639.

When did SONICAID TEAM receive FDA 510(k) clearance?

SONICAID TEAM received FDA 510(k) clearance on 1991-12-31, under 510(k) number K912639.

Who is the listed applicant for SONICAID TEAM?

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

What is the FDA product code for SONICAID TEAM?

The FDA product code for SONICAID TEAM is HGM.

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Other records listing Oxford Medilog, 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.

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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.

K254036Novii+ Wireless Patch SystemDatex Ohmeda, Inc.K253021ANNE MaternalSibel Health, Inc.K250777Sonicaid Team3Huntleigh Healthcare , Ltd.K241882Fetal & Maternal Monitor (F15A, F15A Air)Edan Instruments, Inc.K241368Sonicaid Team3Huntleigh Healthcare , Ltd.K241009PeriCALM Patterns 3.0Perigen, Inc.

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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