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FDA 510(k)

OSTEO OSCILAIR

K-Number: K803284 · 1981-01-09

ApplicantRichard'S Medical Equip., Inc.
Decision Date1981-01-09
Product CodeHSZ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

OSTEO OSCILAIR is the device name listed in this FDA 510(k) record. The listed applicant is Richard'S Medical Equip., Inc.. It received FDA 510(k) clearance on 1981-01-09 under 510(k) number K803284. The device is classified under product code HSZ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OSTEO OSCILAIR?

OSTEO OSCILAIR is a medical device that received FDA 510(k) clearance on 1981-01-09. The listed applicant is Richard'S Medical Equip., Inc.. The 510(k) number is K803284.

When did OSTEO OSCILAIR receive FDA 510(k) clearance?

OSTEO OSCILAIR received FDA 510(k) clearance on 1981-01-09, under 510(k) number K803284.

Who is the listed applicant for OSTEO OSCILAIR?

The FDA 510(k) record lists Richard'S Medical Equip., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for OSTEO OSCILAIR?

The FDA product code for OSTEO OSCILAIR is HSZ.

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Other records listing Richard'S Medical Equip., Inc. as applicant

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Related Devices (Code: HSZ)

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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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