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FDA 510(k)

FAST FLOW #60310

K-Number: K791365 · 1979-09-27

ApplicantHi Chem, Inc.
Decision Date1979-09-27
Product CodeLCP
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

FAST FLOW #60310 is the device name listed in this FDA 510(k) record. The listed applicant is Hi Chem, Inc.. It received FDA 510(k) clearance on 1979-09-27 under 510(k) number K791365. The device is classified under product code LCP. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FAST FLOW #60310?

FAST FLOW #60310 is a medical device that received FDA 510(k) clearance on 1979-09-27. The listed applicant is Hi Chem, Inc.. The 510(k) number is K791365.

When did FAST FLOW #60310 receive FDA 510(k) clearance?

FAST FLOW #60310 received FDA 510(k) clearance on 1979-09-27, under 510(k) number K791365.

Who is the listed applicant for FAST FLOW #60310?

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

What is the FDA product code for FAST FLOW #60310?

The FDA product code for FAST FLOW #60310 is LCP.

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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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