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FDA 510(k)

ADDITIVE CAP (2B8905)

K-Number: K760880 · 1976-12-30

ApplicantTravenol Laboratories, S.A.
Decision Date1976-12-30
Product CodeKPE
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ADDITIVE CAP (2B8905) is the device name listed in this FDA 510(k) record. The listed applicant is Travenol Laboratories, S.A.. It received FDA 510(k) clearance on 1976-12-30 under 510(k) number K760880. 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 CAP (2B8905)?

ADDITIVE CAP (2B8905) is a medical device that received FDA 510(k) clearance on 1976-12-30. The listed applicant is Travenol Laboratories, S.A.. The 510(k) number is K760880.

When did ADDITIVE CAP (2B8905) receive FDA 510(k) clearance?

ADDITIVE CAP (2B8905) received FDA 510(k) clearance on 1976-12-30, under 510(k) number K760880.

Who is the listed applicant for ADDITIVE CAP (2B8905)?

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

What is the FDA product code for ADDITIVE CAP (2B8905)?

The FDA product code for ADDITIVE CAP (2B8905) is KPE.

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Other records listing Travenol Laboratories, S.A. as applicant

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Related Devices (Code: KPE)

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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