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FDA 510(k)

LANCET, BLOOD, STERILE STAINLESS STEEL

K-Number: K760362 · 1976-09-13

ApplicantAeroceuticals
Decision Date1976-09-13
Product CodeKDC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LANCET, BLOOD, STERILE STAINLESS STEEL is the device name listed in this FDA 510(k) record. The listed applicant is Aeroceuticals. It received FDA 510(k) clearance on 1976-09-13 under 510(k) number K760362. 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 LANCET, BLOOD, STERILE STAINLESS STEEL?

LANCET, BLOOD, STERILE STAINLESS STEEL is a medical device that received FDA 510(k) clearance on 1976-09-13. The listed applicant is Aeroceuticals. The 510(k) number is K760362.

When did LANCET, BLOOD, STERILE STAINLESS STEEL receive FDA 510(k) clearance?

LANCET, BLOOD, STERILE STAINLESS STEEL received FDA 510(k) clearance on 1976-09-13, under 510(k) number K760362.

Who is the listed applicant for LANCET, BLOOD, STERILE STAINLESS STEEL?

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

What is the FDA product code for LANCET, BLOOD, STERILE STAINLESS STEEL?

The FDA product code for LANCET, BLOOD, STERILE STAINLESS STEEL is KDC.

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 Aeroceuticals 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.

K770217LANCE LTD. STERI. STITCH CUTTER BLADEK760361BLADE, SURGICAL SCALPEL, STERILEK760363SCALPEL, SURGICAL, STERILE STAINLESSK760364HANDLE, SCALPEL, STAINLESS STEEL

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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