Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

ALEXANDER BOX, BATTERY, RECHARGEABLE

K-Number: K963305 · 1997-04-17

ApplicantAlexander Mfg. Co.
Decision Date1997-04-17
Product CodeBWA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ALEXANDER BOX, BATTERY, RECHARGEABLE is the device name listed in this FDA 510(k) record. The listed applicant is Alexander Mfg. Co.. It received FDA 510(k) clearance on 1997-04-17 under 510(k) number K963305. The device is classified under product code BWA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ALEXANDER BOX, BATTERY, RECHARGEABLE?

ALEXANDER BOX, BATTERY, RECHARGEABLE is a medical device that received FDA 510(k) clearance on 1997-04-17. The listed applicant is Alexander Mfg. Co.. The 510(k) number is K963305.

When did ALEXANDER BOX, BATTERY, RECHARGEABLE receive FDA 510(k) clearance?

ALEXANDER BOX, BATTERY, RECHARGEABLE received FDA 510(k) clearance on 1997-04-17, under 510(k) number K963305.

Who is the listed applicant for ALEXANDER BOX, BATTERY, RECHARGEABLE?

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

What is the FDA product code for ALEXANDER BOX, BATTERY, RECHARGEABLE?

The FDA product code for ALEXANDER BOX, BATTERY, RECHARGEABLE is BWA.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Alexander Mfg. Co. 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.

K982896ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER LP9K981776ALEXANDER MANUFACTURING CO. BATTERY PART NUMBER MC146XK981728ALEXANDER MANUFACTURING CO. BATTERY PART NUMBER H134K980224ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER MS822K974061RECHARGEABLE BATTERY PART NUMBER GL825-200K973851ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY #M12/630

View all 39 devices →

Related Devices (Code: BWA)

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.

K874794E600B FOOTSWITCHValleylab, Inc.K873809EXCALIBUR ELECTROSURGICAL UNIT 60-5200-001Zimmer Aspen Labs

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.

↑