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FDA 510(k)

NEEDLE & BLADE COUNTER

K-Number: K820332 · 1982-02-23

ApplicantAbco Dist.
Decision Date1982-02-23
Product CodeFSM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

NEEDLE & BLADE COUNTER is the device name listed in this FDA 510(k) record. The listed applicant is Abco Dist.. It received FDA 510(k) clearance on 1982-02-23 under 510(k) number K820332. The device is classified under product code FSM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEEDLE & BLADE COUNTER?

NEEDLE & BLADE COUNTER is a medical device that received FDA 510(k) clearance on 1982-02-23. The listed applicant is Abco Dist.. The 510(k) number is K820332.

When did NEEDLE & BLADE COUNTER receive FDA 510(k) clearance?

NEEDLE & BLADE COUNTER received FDA 510(k) clearance on 1982-02-23, under 510(k) number K820332.

Who is the listed applicant for NEEDLE & BLADE COUNTER?

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

What is the FDA product code for NEEDLE & BLADE COUNTER?

The FDA product code for NEEDLE & BLADE COUNTER is FSM.

Related Clinical Trials

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Other records listing Abco Dist. 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.

K820510TYMPANOSTOMY TUBES (VARIOUS MODELS

Related Devices (Code: FSM)

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.

K971217INSTRUMENT TRAY LINERGeneral Hospital Supply Corp.K962328SINGLE USE INSTRUMENT TRAYMedcare Medical Group, Inc.K944025SURGICAL INSTRUMENT TRAYRiley Medical, Inc.K912106ARTHROSCOPY TRAYMedical Device Inspection Co., Inc.K912053OPEN HEART TRAYMedical Device Inspection Co., Inc.K912052HEART CATH TRAYMedical Device Inspection Co., Inc.

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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