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FDA 510(k)

STERNAL POWER AWL

K-Number: K873766 · 1988-11-14

ApplicantBowen & Company, Inc.
Decision Date1988-11-14
Product CodeKIJ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

STERNAL POWER AWL 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 1988-11-14 under 510(k) number K873766. The device is classified under product code KIJ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STERNAL POWER AWL?

STERNAL POWER AWL is a medical device that received FDA 510(k) clearance on 1988-11-14. The listed applicant is Bowen & Company, Inc.. The 510(k) number is K873766.

When did STERNAL POWER AWL receive FDA 510(k) clearance?

STERNAL POWER AWL received FDA 510(k) clearance on 1988-11-14, under 510(k) number K873766.

Who is the listed applicant for STERNAL POWER AWL?

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 STERNAL POWER AWL?

The FDA product code for STERNAL POWER AWL is KIJ.

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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 SHAVERK872098CREMEEN ALVEOLAR BONE CALIPERK871325BOWEN REUSEABLE/DISPOSABLE ELECTRODEK87088245 DEGREE SHAVERK870881LOOSE BODY GRASPERS

View all 14 devices →

Related Devices (Code: KIJ)

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.

K163308SMARTOJeil Medical CorporationK112599INSURGICAL SINGLE USE POWER EQUIPMENTInsurgical, LLCK101563SMARTOJeil Medical CorporationK972367STRYKER SYSTEM 4000 HEAVY DUTY BATTERY POWERED EQUIPMENTStryker InstrumentsK970378STRYKER 2115 REPLACEMENT BATTERY (2115)Implant Resource, Inc.K960711ACUMED BONE GRAFT SYSTEMAcu Med, 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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