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FDA 510(k)

DITTMAR POWER LIFTER

K-Number: K883260 · 1988-11-07

ApplicantDittmar and Penn Corp.
Decision Date1988-11-07
Product CodeFOX
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DITTMAR POWER LIFTER is the device name listed in this FDA 510(k) record. The listed applicant is Dittmar and Penn Corp.. It received FDA 510(k) clearance on 1988-11-07 under 510(k) number K883260. The device is classified under product code FOX. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DITTMAR POWER LIFTER?

DITTMAR POWER LIFTER is a medical device that received FDA 510(k) clearance on 1988-11-07. The listed applicant is Dittmar and Penn Corp.. The 510(k) number is K883260.

When did DITTMAR POWER LIFTER receive FDA 510(k) clearance?

DITTMAR POWER LIFTER received FDA 510(k) clearance on 1988-11-07, under 510(k) number K883260.

Who is the listed applicant for DITTMAR POWER LIFTER?

The FDA 510(k) record lists Dittmar and Penn Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DITTMAR POWER LIFTER?

The FDA product code for DITTMAR POWER LIFTER is FOX.

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 Dittmar and Penn Corp. 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.

K864953WEIGHMOBILE, IN BED PATIENT WEIGHING SCALE

Related Devices (Code: FOX)

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.

K980336IV STANDSClinton Industries, Inc.K964782MEDRAD CONTRAST HOLDERMedrad, Inc.K961470PORT-A-POLEPrins Medical Ind., Inc.K960027HIGH VOLUME I.V. & IRRIGATION TOWERAllen Medical Systems, Inc.K952196IV POLE/STANDValentine Intl. , Ltd.K950367IV SHUTTLEEquipment Concepts, 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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