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FDA 510(k)

MORGAN ARTHROSCOPIC MENESUS & SYNOVIAL RASP

K-Number: K853601 · 1985-09-16

ApplicantBowen & Company, Inc.
Decision Date1985-09-16
Product CodeGAC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MORGAN ARTHROSCOPIC MENESUS & SYNOVIAL RASP is the device name listed in this FDA 510(k) record. The listed applicant is Bowen & Company, Inc.. It received FDA 510(k) clearance on 1985-09-16 under 510(k) number K853601. The device is classified under product code GAC. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MORGAN ARTHROSCOPIC MENESUS & SYNOVIAL RASP?

MORGAN ARTHROSCOPIC MENESUS & SYNOVIAL RASP is a medical device that received FDA 510(k) clearance on 1985-09-16. The listed applicant is Bowen & Company, Inc.. The 510(k) number is K853601.

When did MORGAN ARTHROSCOPIC MENESUS & SYNOVIAL RASP receive FDA 510(k) clearance?

MORGAN ARTHROSCOPIC MENESUS & SYNOVIAL RASP received FDA 510(k) clearance on 1985-09-16, under 510(k) number K853601.

Who is the listed applicant for MORGAN ARTHROSCOPIC MENESUS & SYNOVIAL RASP?

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

What is the FDA product code for MORGAN ARTHROSCOPIC MENESUS & SYNOVIAL RASP?

The FDA product code for MORGAN ARTHROSCOPIC MENESUS & SYNOVIAL RASP is GAC.

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Other records listing Bowen & Company, 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.

K896898BOWEN ELECTRODE SKIN PREPATORY CLEANSERK896538DISPOSABLE 45 DEGREE SHAVERK873766STERNAL POWER AWLK872098CREMEEN ALVEOLAR BONE CALIPERK871325BOWEN REUSEABLE/DISPOSABLE ELECTRODEK87088245 DEGREE SHAVER

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Related Devices (Code: GAC)

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

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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