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FDA 510(k)

ABC HANDPIECE ADAPTER

K-Number: K901248 · 1990-04-03

ApplicantBeacon Laboratories, Inc.
Decision Date1990-04-03
Product CodeHAM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ABC HANDPIECE ADAPTER is the device name listed in this FDA 510(k) record. The listed applicant is Beacon Laboratories, Inc.. It received FDA 510(k) clearance on 1990-04-03 under 510(k) number K901248. The device is classified under product code HAM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ABC HANDPIECE ADAPTER?

ABC HANDPIECE ADAPTER is a medical device that received FDA 510(k) clearance on 1990-04-03. The listed applicant is Beacon Laboratories, Inc.. The 510(k) number is K901248.

When did ABC HANDPIECE ADAPTER receive FDA 510(k) clearance?

ABC HANDPIECE ADAPTER received FDA 510(k) clearance on 1990-04-03, under 510(k) number K901248.

Who is the listed applicant for ABC HANDPIECE ADAPTER?

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

What is the FDA product code for ABC HANDPIECE ADAPTER?

The FDA product code for ABC HANDPIECE ADAPTER is HAM.

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Other records listing Beacon Laboratories, 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.

K930243FLEXIBLE EXTENDERK930497ARGON HANDPIECESK925708DISPOSABLE ELECTROSURGERY BALL ELECTRODEK922289SESQUIPOLAR(TM) MIS ELECTRODEK925619DISPOSABLE HAND-SWITCHING ESU PENCILK915788MIS ELECTROSURGICAL ELECTRODES

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Related Devices (Code: HAM)

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.

K153472Quiver Laparoscopic ExtendableItl Corporation Pty, Ltd.K000079NIKOPAD ELECTROSURGICAL GROUNDING PAD, MODEL 4777MNikomed U.S.A., Inc.K993306NIKOPAD ELECTROSURGICAL GROUNDING PAD (*OR SOLD UNDER COMMERCIAL NAMES), MODEL 4760 (TYPICALLY)Paladin Medical, Inc.K945861BERGEN 710 ESUBergen Mfg.K913300LAPAROSTAT(TM)Cook Ob/GynK920100GSU HANDPIECE ADAPTERBeacon Laboratories, 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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