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FDA 510(k)

STOCKINETTE, SURGICAL

K-Number: K770621 · 1977-04-06

ApplicantThe Torrent Corp.
Decision Date1977-04-06
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

STOCKINETTE, SURGICAL is the device name listed in this FDA 510(k) record. The listed applicant is The Torrent Corp.. It received FDA 510(k) clearance on 1977-04-06 under 510(k) number K770621. The device is classified under product code KKX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STOCKINETTE, SURGICAL?

STOCKINETTE, SURGICAL is a medical device that received FDA 510(k) clearance on 1977-04-06. The listed applicant is The Torrent Corp.. The 510(k) number is K770621.

When did STOCKINETTE, SURGICAL receive FDA 510(k) clearance?

STOCKINETTE, SURGICAL received FDA 510(k) clearance on 1977-04-06, under 510(k) number K770621.

Who is the listed applicant for STOCKINETTE, SURGICAL?

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

What is the FDA product code for STOCKINETTE, SURGICAL?

The FDA product code for STOCKINETTE, SURGICAL is KKX.

Related Clinical Trials

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Other records listing The Torrent Corp. 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.

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Related Devices (Code: KKX)

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

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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