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FDA 510(k)

RELEASABLE FORCE MODULE

K-Number: K980151 · 1998-04-06

Decision Date1998-04-06
Product CodeDZB
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

RELEASABLE FORCE MODULE is the device name listed in this FDA 510(k) record. The listed applicant is Ortho Kinetics Corp.. It received FDA 510(k) clearance on 1998-04-06 under 510(k) number K980151. The device is classified under product code DZB. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RELEASABLE FORCE MODULE?

RELEASABLE FORCE MODULE is a medical device that received FDA 510(k) clearance on 1998-04-06. The listed applicant is Ortho Kinetics Corp.. The 510(k) number is K980151.

When did RELEASABLE FORCE MODULE receive FDA 510(k) clearance?

RELEASABLE FORCE MODULE received FDA 510(k) clearance on 1998-04-06, under 510(k) number K980151.

Who is the listed applicant for RELEASABLE FORCE MODULE?

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

What is the FDA product code for RELEASABLE FORCE MODULE?

The FDA product code for RELEASABLE FORCE MODULE is DZB.

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.

Other records listing Ortho Kinetics Corp. 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.

View all 7 devices →

Related Devices (Code: DZB)

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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