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FDA 510(k)

APRON, LEADED VINYL

K-Number: K790080 · 1979-01-26

ApplicantPinnacle Distributors, Inc.
Decision Date1979-01-26
Product CodeKPY
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

APRON, LEADED VINYL is the device name listed in this FDA 510(k) record. The listed applicant is Pinnacle Distributors, Inc.. It received FDA 510(k) clearance on 1979-01-26 under 510(k) number K790080. The device is classified under product code KPY. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the APRON, LEADED VINYL?

APRON, LEADED VINYL is a medical device that received FDA 510(k) clearance on 1979-01-26. The listed applicant is Pinnacle Distributors, Inc.. The 510(k) number is K790080.

When did APRON, LEADED VINYL receive FDA 510(k) clearance?

APRON, LEADED VINYL received FDA 510(k) clearance on 1979-01-26, under 510(k) number K790080.

Who is the listed applicant for APRON, LEADED VINYL?

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

What is the FDA product code for APRON, LEADED VINYL?

The FDA product code for APRON, LEADED VINYL is KPY.

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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Other records listing Pinnacle Distributors, Inc. 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.

K781852GLOVE, SUPERFLEX MOLDED

Related Devices (Code: KPY)

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.

K110900DISPOSABLE THYROID COLLARBloxr CorporationK962622INTRA-ORAL THERMOPLASTIC SHIELDMedtec, Inc.K954456THERMOPLASTIC SHIELDMedtec, Inc.K954146UTK-DTE AUTILARY SHIELDMallinckrodt MedicalK953610AUKULYTEAukland Medical Plastics, Inc.K9510042001 SPECIAL PROCEDURE LAMP (LOW VOLTAGE) (AS EXHIBITS #2 & 4)Kenex , Ltd.

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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