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FDA 510(k)

LATERAL POSITIONING ATTACHMENT

K-Number: K830443 · 1983-03-10

ApplicantBerivon Co.
Decision Date1983-03-10
Product Code
DecisionSubstantially Equivalent

Device Summary

LATERAL POSITIONING ATTACHMENT is the device name listed in this FDA 510(k) record. The listed applicant is Berivon Co.. It received FDA 510(k) clearance on 1983-03-10 under 510(k) number K830443. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LATERAL POSITIONING ATTACHMENT?

LATERAL POSITIONING ATTACHMENT is a medical device that received FDA 510(k) clearance on 1983-03-10. The listed applicant is Berivon Co.. The 510(k) number is K830443.

When did LATERAL POSITIONING ATTACHMENT receive FDA 510(k) clearance?

LATERAL POSITIONING ATTACHMENT received FDA 510(k) clearance on 1983-03-10, under 510(k) number K830443.

Who is the listed applicant for LATERAL POSITIONING ATTACHMENT?

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

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.

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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