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FDA 510(k)

CRAWFORD PORTAVAC

K-Number: K760664 · 1976-10-05

ApplicantCrawford Electric
Decision Date1976-10-05
Product Code
DecisionSubstantially Equivalent

Device Summary

CRAWFORD PORTAVAC is the device name listed in this FDA 510(k) record. The listed applicant is Crawford Electric. It received FDA 510(k) clearance on 1976-10-05 under 510(k) number K760664. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CRAWFORD PORTAVAC?

CRAWFORD PORTAVAC is a medical device that received FDA 510(k) clearance on 1976-10-05. The listed applicant is Crawford Electric. The 510(k) number is K760664.

When did CRAWFORD PORTAVAC receive FDA 510(k) clearance?

CRAWFORD PORTAVAC received FDA 510(k) clearance on 1976-10-05, under 510(k) number K760664.

Who is the listed applicant for CRAWFORD PORTAVAC?

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

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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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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