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FDA 510(k)

SIMVAC

K-Number: K811991 · 1981-08-12

ApplicantThe Lynn Terrell Co.
Decision Date1981-08-12
Product CodeCBO
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SIMVAC is the device name listed in this FDA 510(k) record. The listed applicant is The Lynn Terrell Co.. It received FDA 510(k) clearance on 1981-08-12 under 510(k) number K811991. The device is classified under product code CBO. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIMVAC?

SIMVAC is a medical device that received FDA 510(k) clearance on 1981-08-12. The listed applicant is The Lynn Terrell Co.. The 510(k) number is K811991.

When did SIMVAC receive FDA 510(k) clearance?

SIMVAC received FDA 510(k) clearance on 1981-08-12, under 510(k) number K811991.

Who is the listed applicant for SIMVAC?

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

What is the FDA product code for SIMVAC?

The FDA product code for SIMVAC is CBO.

Related Clinical Trials

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Related Devices (Code: CBO)

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.

K811908IMV MANIFOLDSAirlife, Inc.K791904IMV W/BAG & HOSES #M-509Mem Medical, Inc.K791913IMV MANIFOLD #M-506Mem Medical, Inc.K791909IMV BUSHING #M-513Mem Medical, Inc.K791912IMV FOR MONITORING #M-510Mem Medical, Inc.K791905IMV W/BAG & TUBING #M-508Mem Medical, Inc.

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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