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FDA 510(k)

PLASTER VACUUM, 115V MODEL NO. 4183-160

K-Number: K873721 · 1987-12-07

ApplicantMartin Medical
Decision Date1987-12-07
Product CodeLGH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

PLASTER VACUUM, 115V MODEL NO. 4183-160 is the device name listed in this FDA 510(k) record. The listed applicant is Martin Medical. It received FDA 510(k) clearance on 1987-12-07 under 510(k) number K873721. 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 PLASTER VACUUM, 115V MODEL NO. 4183-160?

PLASTER VACUUM, 115V MODEL NO. 4183-160 is a medical device that received FDA 510(k) clearance on 1987-12-07. The listed applicant is Martin Medical. The 510(k) number is K873721.

When did PLASTER VACUUM, 115V MODEL NO. 4183-160 receive FDA 510(k) clearance?

PLASTER VACUUM, 115V MODEL NO. 4183-160 received FDA 510(k) clearance on 1987-12-07, under 510(k) number K873721.

Who is the listed applicant for PLASTER VACUUM, 115V MODEL NO. 4183-160?

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

What is the FDA product code for PLASTER VACUUM, 115V MODEL NO. 4183-160?

The FDA product code for PLASTER VACUUM, 115V MODEL NO. 4183-160 is LGH.

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Other records listing Martin Medical 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.

K873723PLASTER VACUUM, 230V MODEL NO. 4183-161K873719CAST CUTTER, 115V MODEL NO. 4183-106K873722PEDESTAL WALKING HEEL PRODUCT NO. 4183-133K873720CAST CUTTER, 230V MODEL NO. 4183-107K873716ADULT WALKING HEEL PRODUCT NO. 4183-130K873717CUSHION TREAD WALKING HEEL PRODUCT NO. 4183-135

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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.K895861DELTA-TECH(TM) CAST REMOVAL SYSTEMJohnson & Johnson Professionals, Inc.K873723PLASTER VACUUM, 230V MODEL NO. 4183-161Martin 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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