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FDA 510(k)

HEELBO PELVIC RESTRAINT

K-Number: K963199 · 1996-11-01

Decision Date1996-11-01
Product CodeFMQ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

HEELBO PELVIC RESTRAINT is the device name listed in this FDA 510(k) record. The listed applicant is Hollister, Inc.. It received FDA 510(k) clearance on 1996-11-01 under 510(k) number K963199. 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 HEELBO PELVIC RESTRAINT?

HEELBO PELVIC RESTRAINT is a medical device that received FDA 510(k) clearance on 1996-11-01. The listed applicant is Hollister, Inc.. The 510(k) number is K963199.

When did HEELBO PELVIC RESTRAINT receive FDA 510(k) clearance?

HEELBO PELVIC RESTRAINT received FDA 510(k) clearance on 1996-11-01, under 510(k) number K963199.

Who is the listed applicant for HEELBO PELVIC RESTRAINT?

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

What is the FDA product code for HEELBO PELVIC RESTRAINT?

The FDA product code for HEELBO PELVIC RESTRAINT is FMQ.

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.

Other records listing Hollister, Inc. 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.

View all 85 devices →

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.

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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