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FDA 510(k)

STRETCHER, WHEELED, MECHANICAL

K-Number: K873181 · 1987-10-09

Decision Date1987-10-09
Product CodeFPO
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

STRETCHER, WHEELED, MECHANICAL is the device name listed in this FDA 510(k) record. The listed applicant is Cambridge Technologies, Inc.. It received FDA 510(k) clearance on 1987-10-09 under 510(k) number K873181. 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 STRETCHER, WHEELED, MECHANICAL?

STRETCHER, WHEELED, MECHANICAL is a medical device that received FDA 510(k) clearance on 1987-10-09. The listed applicant is Cambridge Technologies, Inc.. The 510(k) number is K873181.

When did STRETCHER, WHEELED, MECHANICAL receive FDA 510(k) clearance?

STRETCHER, WHEELED, MECHANICAL received FDA 510(k) clearance on 1987-10-09, under 510(k) number K873181.

Who is the listed applicant for STRETCHER, WHEELED, MECHANICAL?

The FDA 510(k) record lists Cambridge Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STRETCHER, WHEELED, MECHANICAL?

The FDA product code for STRETCHER, WHEELED, MECHANICAL 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 Cambridge Technologies, Inc. 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.

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

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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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