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FDA 510(k)

NOVABED PATIENT TRANSFER SYSTEM

K-Number: K964246 · 1997-01-22

ApplicantNova Technology Corp.
Decision Date1997-01-22
Product CodeFNL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

NOVABED PATIENT TRANSFER SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Nova Technology Corp.. It received FDA 510(k) clearance on 1997-01-22 under 510(k) number K964246. The device is classified under product code FNL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NOVABED PATIENT TRANSFER SYSTEM?

NOVABED PATIENT TRANSFER SYSTEM is a medical device that received FDA 510(k) clearance on 1997-01-22. The listed applicant is Nova Technology Corp.. The 510(k) number is K964246.

When did NOVABED PATIENT TRANSFER SYSTEM receive FDA 510(k) clearance?

NOVABED PATIENT TRANSFER SYSTEM received FDA 510(k) clearance on 1997-01-22, under 510(k) number K964246.

Who is the listed applicant for NOVABED PATIENT TRANSFER SYSTEM?

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

What is the FDA product code for NOVABED PATIENT TRANSFER SYSTEM?

The FDA product code for NOVABED PATIENT TRANSFER SYSTEM is FNL.

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.

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Other records listing Nova Technology 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.

K963701SOMA SAFE ENCLOSUREK874448NOVA TRANSFER SYSTEM, MODEL XXX

Related Devices (Code: FNL)

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

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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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