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FDA 510(k)

NEO-FLOAT NEONATAL FLOTATION SYS & RHYT

K-Number: K832829 · 1983-10-04

ApplicantClinical Data Instruments, Inc.
Decision Date1983-10-04
Product CodeIOQ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

NEO-FLOAT NEONATAL FLOTATION SYS & RHYT is the device name listed in this FDA 510(k) record. The listed applicant is Clinical Data Instruments, Inc.. It received FDA 510(k) clearance on 1983-10-04 under 510(k) number K832829. The device is classified under product code IOQ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEO-FLOAT NEONATAL FLOTATION SYS & RHYT?

NEO-FLOAT NEONATAL FLOTATION SYS & RHYT is a medical device that received FDA 510(k) clearance on 1983-10-04. The listed applicant is Clinical Data Instruments, Inc.. The 510(k) number is K832829.

When did NEO-FLOAT NEONATAL FLOTATION SYS & RHYT receive FDA 510(k) clearance?

NEO-FLOAT NEONATAL FLOTATION SYS & RHYT received FDA 510(k) clearance on 1983-10-04, under 510(k) number K832829.

Who is the listed applicant for NEO-FLOAT NEONATAL FLOTATION SYS & RHYT?

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

What is the FDA product code for NEO-FLOAT NEONATAL FLOTATION SYS & RHYT?

The FDA product code for NEO-FLOAT NEONATAL FLOTATION SYS & RHYT is IOQ.

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Other records listing Clinical Data Instruments, 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.

K842349AMBULATORY PH RECORDING DEVICEK832828CENTURION CARDIAC DETECTOR

Related Devices (Code: IOQ)

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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Official Source

View on FDA Database →

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