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FDA 510(k)

MASSAPED

K-Number: K842643 · 1984-07-25

ApplicantHeddernheimer Metallwarenfabrik GmbH
Decision Date1984-07-25
Product CodeILJ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MASSAPED is the device name listed in this FDA 510(k) record. The listed applicant is Heddernheimer Metallwarenfabrik GmbH. It received FDA 510(k) clearance on 1984-07-25 under 510(k) number K842643. The device is classified under product code ILJ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MASSAPED?

MASSAPED is a medical device that received FDA 510(k) clearance on 1984-07-25. The listed applicant is Heddernheimer Metallwarenfabrik GmbH. The 510(k) number is K842643.

When did MASSAPED receive FDA 510(k) clearance?

MASSAPED received FDA 510(k) clearance on 1984-07-25, under 510(k) number K842643.

Who is the listed applicant for MASSAPED?

The FDA 510(k) record lists Heddernheimer Metallwarenfabrik GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MASSAPED?

The FDA product code for MASSAPED is ILJ.

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 Heddernheimer Metallwarenfabrik GmbH 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.

K842642BALSAN 700K842641HYDRO/BUBBLE BATH DEVICE 300

Related Devices (Code: ILJ)

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.

K110994PARKER 500Arjohuntleigh, Inc.K082951IMMERSION HYDROBATHArjo Hospital Equipment ABK052479MBATH 1000 (60)Enneking Medical, Inc.K040772PACIFIC RECUMBENT HEIGHT-ADJUSTABLE BATH SYSTEMPenner Manufacturing, Inc.K012057CASCADE BATH, MODEL 6900Penner Manufacturing, Inc.K012061SUPERIOR BATH, MODEL 6300Penner Manufacturing, 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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