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)

NDM DIATEMP INFANT ELECTROSURG. DISP. P.

K-Number: K810920 · 1981-05-01

ApplicantNdm Corp.
Decision Date1981-05-01
Product CodeHAM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

NDM DIATEMP INFANT ELECTROSURG. DISP. P. is the device name listed in this FDA 510(k) record. The listed applicant is Ndm Corp.. It received FDA 510(k) clearance on 1981-05-01 under 510(k) number K810920. The device is classified under product code HAM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NDM DIATEMP INFANT ELECTROSURG. DISP. P.?

NDM DIATEMP INFANT ELECTROSURG. DISP. P. is a medical device that received FDA 510(k) clearance on 1981-05-01. The listed applicant is Ndm Corp.. The 510(k) number is K810920.

When did NDM DIATEMP INFANT ELECTROSURG. DISP. P. receive FDA 510(k) clearance?

NDM DIATEMP INFANT ELECTROSURG. DISP. P. received FDA 510(k) clearance on 1981-05-01, under 510(k) number K810920.

Who is the listed applicant for NDM DIATEMP INFANT ELECTROSURG. DISP. P.?

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

What is the FDA product code for NDM DIATEMP INFANT ELECTROSURG. DISP. P.?

The FDA product code for NDM DIATEMP INFANT ELECTROSURG. DISP. P. is HAM.

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 Ndm 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.

K926202CLEARSITE STERILE WOUND DRESSING, NDM WOUND DRESSIK901145NDM SWITCHPEN HOLSTERK853968DIATEMP ELECTROSURGICAL PENK830663PENCIL SKIN ABRADERK801158NDM DIATEMP ELECTROSURGICAL DIS. PADK790730NDM PAPER TAPE ECG ELECTRODE

View all 11 devices →

Related Devices (Code: HAM)

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.

K153472Quiver Laparoscopic ExtendableItl Corporation Pty, Ltd.K000079NIKOPAD ELECTROSURGICAL GROUNDING PAD, MODEL 4777MNikomed U.S.A., Inc.K993306NIKOPAD ELECTROSURGICAL GROUNDING PAD (*OR SOLD UNDER COMMERCIAL NAMES), MODEL 4760 (TYPICALLY)Paladin Medical, Inc.K945861BERGEN 710 ESUBergen Mfg.K913300LAPAROSTAT(TM)Cook Ob/GynK920100GSU HANDPIECE ADAPTERBeacon Laboratories, 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.

↑