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FDA 510(k)

GINGI-PLAIN CORDS & BRAIDS

K-Number: K812120 · 1981-09-08

ApplicantBelport Co., Inc.
Decision Date1981-09-08
Product CodeJES
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

GINGI-PLAIN CORDS & BRAIDS is the device name listed in this FDA 510(k) record. The listed applicant is Belport Co., Inc.. It received FDA 510(k) clearance on 1981-09-08 under 510(k) number K812120. The device is classified under product code JES. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GINGI-PLAIN CORDS & BRAIDS?

GINGI-PLAIN CORDS & BRAIDS is a medical device that received FDA 510(k) clearance on 1981-09-08. The listed applicant is Belport Co., Inc.. The 510(k) number is K812120.

When did GINGI-PLAIN CORDS & BRAIDS receive FDA 510(k) clearance?

GINGI-PLAIN CORDS & BRAIDS received FDA 510(k) clearance on 1981-09-08, under 510(k) number K812120.

Who is the listed applicant for GINGI-PLAIN CORDS & BRAIDS?

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

What is the FDA product code for GINGI-PLAIN CORDS & BRAIDS?

The FDA product code for GINGI-PLAIN CORDS & BRAIDS is JES.

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Other records listing Belport Co., 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.

K820061REVERSIBLE HYDROCOLLOID IMPRESSION MAT

Related Devices (Code: JES)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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