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FDA 510(k)

SAFETY PINS & RUBBER BANDS

K-Number: K831915 · 1983-09-12

ApplicantOrmed Mfg., Inc.
Decision Date1983-09-12
Product CodeKDC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SAFETY PINS & RUBBER BANDS is the device name listed in this FDA 510(k) record. The listed applicant is Ormed Mfg., Inc.. It received FDA 510(k) clearance on 1983-09-12 under 510(k) number K831915. The device is classified under product code KDC. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SAFETY PINS & RUBBER BANDS?

SAFETY PINS & RUBBER BANDS is a medical device that received FDA 510(k) clearance on 1983-09-12. The listed applicant is Ormed Mfg., Inc.. The 510(k) number is K831915.

When did SAFETY PINS & RUBBER BANDS receive FDA 510(k) clearance?

SAFETY PINS & RUBBER BANDS received FDA 510(k) clearance on 1983-09-12, under 510(k) number K831915.

Who is the listed applicant for SAFETY PINS & RUBBER BANDS?

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

What is the FDA product code for SAFETY PINS & RUBBER BANDS?

The FDA product code for SAFETY PINS & RUBBER BANDS is KDC.

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Other records listing Ormed Mfg., 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.

K931555ARTROMOT K2 CPMK882529BUTCHER STRUNG TONSIL SPONGEK882527GAUZE SPONGEK882528CYLINDRICAL SPONGEK882530TAPE STRUNG TONSIL SPONGEK880853CHERRY SPONGE

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Related Devices (Code: KDC)

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.

K943229DISPOSABLE SURGICAL SCISSORS AND FORCEPSY.M.K. International Co., Ltd.K936226SURGIMED BREAST LOCALIZATION NEEDLE WIRE SETMeadox Medicals, Div. Boston Scientific Corp.K920153THERMUFF BAGTechstylesK920263MANUAL SURGICAL INSTRUMENTSPhoenix Instruments Div.K915064DISPOSABLE CAUTERY ABRASIVE PADAmerican Medical Mfg., Inc.K914960INSTRUMENT ORGANIZERO.R. Concepts, Inc.

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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