FDA 510(k)

VENT-A-CAST

K-Number: K843780 · 1984-11-14

Decision Date1984-11-14

Product CodeLGF

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

VENT-A-CAST is the device name listed in this FDA 510(k) record. The listed applicant is Orthopedic Technology, Inc.. It received FDA 510(k) clearance on 1984-11-14 under 510(k) number K843780. The device is classified under product code LGF. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VENT-A-CAST?

VENT-A-CAST is a medical device that received FDA 510(k) clearance on 1984-11-14. The listed applicant is Orthopedic Technology, Inc.. The 510(k) number is K843780.

When did VENT-A-CAST receive FDA 510(k) clearance?

VENT-A-CAST received FDA 510(k) clearance on 1984-11-14, under 510(k) number K843780.

Who is the listed applicant for VENT-A-CAST?

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

What is the FDA product code for VENT-A-CAST?

The FDA product code for VENT-A-CAST is LGF.

Other records listing Orthopedic Technology, 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.

K940429ORTHO TECH CRYOLOGIC SYSTEM

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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.