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FDA 510(k)

ADDITIVE HINGE CAP

K-Number: K791796 · 1979-10-01

ApplicantAbbott Laboratories
Decision Date1979-10-01
Product CodeKPE
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ADDITIVE HINGE CAP is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1979-10-01 under 510(k) number K791796. The device is classified under product code KPE. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADDITIVE HINGE CAP?

ADDITIVE HINGE CAP is a medical device that received FDA 510(k) clearance on 1979-10-01. The listed applicant is Abbott Laboratories. The 510(k) number is K791796.

When did ADDITIVE HINGE CAP receive FDA 510(k) clearance?

ADDITIVE HINGE CAP received FDA 510(k) clearance on 1979-10-01, under 510(k) number K791796.

Who is the listed applicant for ADDITIVE HINGE CAP?

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

What is the FDA product code for ADDITIVE HINGE CAP?

The FDA product code for ADDITIVE HINGE CAP is KPE.

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Related Devices (Code: KPE)

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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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