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FDA 510(k)

STRETCHER TRANSIT ISOLATER #122

K-Number: K790657 · 1979-07-03

ApplicantVickers America Medical Corp.
Decision Date1979-07-03
Product CodeLGM
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

STRETCHER TRANSIT ISOLATER #122 is the device name listed in this FDA 510(k) record. The listed applicant is Vickers America Medical Corp.. It received FDA 510(k) clearance on 1979-07-03 under 510(k) number K790657. The device is classified under product code LGM. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STRETCHER TRANSIT ISOLATER #122?

STRETCHER TRANSIT ISOLATER #122 is a medical device that received FDA 510(k) clearance on 1979-07-03. The listed applicant is Vickers America Medical Corp.. The 510(k) number is K790657.

When did STRETCHER TRANSIT ISOLATER #122 receive FDA 510(k) clearance?

STRETCHER TRANSIT ISOLATER #122 received FDA 510(k) clearance on 1979-07-03, under 510(k) number K790657.

Who is the listed applicant for STRETCHER TRANSIT ISOLATER #122?

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

What is the FDA product code for STRETCHER TRANSIT ISOLATER #122?

The FDA product code for STRETCHER TRANSIT ISOLATER #122 is LGM.

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Other records listing Vickers America Medical Corp. as applicant

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Related Devices (Code: LGM)

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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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