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FDA 510(k)

CENTURIAN HYDRAULIC STRETCHER

K-Number: K843439 · 1984-09-13

Decision Date1984-09-13
Product CodeFPO
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CENTURIAN HYDRAULIC STRETCHER is the device name listed in this FDA 510(k) record. The listed applicant is American Sterilizer Co.. It received FDA 510(k) clearance on 1984-09-13 under 510(k) number K843439. The device is classified under product code FPO. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CENTURIAN HYDRAULIC STRETCHER?

CENTURIAN HYDRAULIC STRETCHER is a medical device that received FDA 510(k) clearance on 1984-09-13. The listed applicant is American Sterilizer Co.. The 510(k) number is K843439.

When did CENTURIAN HYDRAULIC STRETCHER receive FDA 510(k) clearance?

CENTURIAN HYDRAULIC STRETCHER received FDA 510(k) clearance on 1984-09-13, under 510(k) number K843439.

Who is the listed applicant for CENTURIAN HYDRAULIC STRETCHER?

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

What is the FDA product code for CENTURIAN HYDRAULIC STRETCHER?

The FDA product code for CENTURIAN HYDRAULIC STRETCHER is FPO.

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 American Sterilizer Co. 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 36 devices →

Related Devices (Code: FPO)

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

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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