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FDA 510(k)

DELTA-TECH(TM) CAST REMOVAL SYSTEM

K-Number: K895861 · 1989-10-19

ApplicantJohnson & Johnson Professionals, Inc.
Decision Date1989-10-19
Product CodeLGH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

DELTA-TECH(TM) CAST REMOVAL SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Johnson & Johnson Professionals, Inc.. It received FDA 510(k) clearance on 1989-10-19 under 510(k) number K895861. The device is classified under product code LGH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DELTA-TECH(TM) CAST REMOVAL SYSTEM?

DELTA-TECH(TM) CAST REMOVAL SYSTEM is a medical device that received FDA 510(k) clearance on 1989-10-19. The listed applicant is Johnson & Johnson Professionals, Inc.. The 510(k) number is K895861.

When did DELTA-TECH(TM) CAST REMOVAL SYSTEM receive FDA 510(k) clearance?

DELTA-TECH(TM) CAST REMOVAL SYSTEM received FDA 510(k) clearance on 1989-10-19, under 510(k) number K895861.

Who is the listed applicant for DELTA-TECH(TM) CAST REMOVAL SYSTEM?

The FDA 510(k) record lists Johnson & Johnson Professionals, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DELTA-TECH(TM) CAST REMOVAL SYSTEM?

The FDA product code for DELTA-TECH(TM) CAST REMOVAL SYSTEM is LGH.

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Other records listing Johnson & Johnson Professionals, Inc. as applicant

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Related Devices (Code: LGH)

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.

K932653SWISSTEK 2000(TM) CAST REMOVAL SYSTEMCarapace, Inc.K901677CARAPACE PORTABLE CAST SAW, SWISS-EX CAST CUTTERBuckman Co., Inc.K893380QCR SYSTEM I AND QCR SYSTEM IIBremer Mfg. & Tool Co., Inc.K873723PLASTER VACUUM, 230V MODEL NO. 4183-161Martin MedicalK873721PLASTER VACUUM, 115V MODEL NO. 4183-160Martin MedicalK873720CAST CUTTER, 230V MODEL NO. 4183-107Martin Medical

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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