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FDA 510(k)

CHILD WALKING HEEL PRODUCT NO. 4183-132

K-Number: K873718 · 1987-10-02

ApplicantMartin Medical
Decision Date1987-10-02
Product CodeLGF
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CHILD WALKING HEEL PRODUCT NO. 4183-132 is the device name listed in this FDA 510(k) record. The listed applicant is Martin Medical. It received FDA 510(k) clearance on 1987-10-02 under 510(k) number K873718. The device is classified under product code LGF. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHILD WALKING HEEL PRODUCT NO. 4183-132?

CHILD WALKING HEEL PRODUCT NO. 4183-132 is a medical device that received FDA 510(k) clearance on 1987-10-02. The listed applicant is Martin Medical. The 510(k) number is K873718.

When did CHILD WALKING HEEL PRODUCT NO. 4183-132 receive FDA 510(k) clearance?

CHILD WALKING HEEL PRODUCT NO. 4183-132 received FDA 510(k) clearance on 1987-10-02, under 510(k) number K873718.

Who is the listed applicant for CHILD WALKING HEEL PRODUCT NO. 4183-132?

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 CHILD WALKING HEEL PRODUCT NO. 4183-132?

The FDA product code for CHILD WALKING HEEL PRODUCT NO. 4183-132 is LGF.

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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. 4183-161K873721PLASTER VACUUM, 115V MODEL NO. 4183-160K873722PEDESTAL WALKING HEEL PRODUCT NO. 4183-133K873716ADULT WALKING HEEL PRODUCT NO. 4183-130K873719CAST CUTTER, 115V MODEL NO. 4183-106K873720CAST CUTTER, 230V MODEL NO. 4183-107

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Related Devices (Code: LGF)

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.

K043526SILVERSEAL TUBULAR WOUND DRESSING WITH X-STATICNoble Fiber Technologies, Inc.K973417CLINITEX STOCKINETTEClinitex Medical Corp.K973420CLINITEX CAST PADDINGClinitex Medical Corp.K955320PROTEC COTTON PADDING BANDAGEDerivadas Degasa S.A. DE C.V.K932507QUICK-CAST IMMOBILIZERLandec Corp.K931672CARAPACE STERILE CAST PADDINGCarapace, 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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