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FDA 510(k)

SPIDER STRAP

K-Number: K963138 · 1996-11-06

ApplicantBdm Medical, Inc.
Decision Date1996-11-06
Product CodeFMQ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SPIDER STRAP is the device name listed in this FDA 510(k) record. The listed applicant is Bdm Medical, Inc.. It received FDA 510(k) clearance on 1996-11-06 under 510(k) number K963138. The device is classified under product code FMQ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPIDER STRAP?

SPIDER STRAP is a medical device that received FDA 510(k) clearance on 1996-11-06. The listed applicant is Bdm Medical, Inc.. The 510(k) number is K963138.

When did SPIDER STRAP receive FDA 510(k) clearance?

SPIDER STRAP received FDA 510(k) clearance on 1996-11-06, under 510(k) number K963138.

Who is the listed applicant for SPIDER STRAP?

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

What is the FDA product code for SPIDER STRAP?

The FDA product code for SPIDER STRAP is FMQ.

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Related Devices (Code: FMQ)

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.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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