FDA 510(k)

HYPO-GRIP

K-Number: K780884 · 1978-08-10

Decision Date1978-08-10

Product CodeKZA

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

HYPO-GRIP is the device name listed in this FDA 510(k) record. The listed applicant is Harco Products. It received FDA 510(k) clearance on 1978-08-10 under 510(k) number K780884. The device is classified under product code KZA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HYPO-GRIP?

HYPO-GRIP is a medical device that received FDA 510(k) clearance on 1978-08-10. The listed applicant is Harco Products. The 510(k) number is K780884.

When did HYPO-GRIP receive FDA 510(k) clearance?

HYPO-GRIP received FDA 510(k) clearance on 1978-08-10, under 510(k) number K780884.

Who is the listed applicant for HYPO-GRIP?

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

What is the FDA product code for HYPO-GRIP?

The FDA product code for HYPO-GRIP is KZA.

Other records listing Harco Products 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.

K780883E-Z-JECTOR

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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.