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FDA 510(k)

GUSBERG HYSTERECTOMY CLAMP

K-Number: K771344 · 1977-07-27

ApplicantJ. Sklar Mfg. Co., Inc.
Decision Date1977-07-27
Product CodeHGC
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

GUSBERG HYSTERECTOMY CLAMP is the device name listed in this FDA 510(k) record. The listed applicant is J. Sklar Mfg. Co., Inc.. It received FDA 510(k) clearance on 1977-07-27 under 510(k) number K771344. The device is classified under product code HGC. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GUSBERG HYSTERECTOMY CLAMP?

GUSBERG HYSTERECTOMY CLAMP is a medical device that received FDA 510(k) clearance on 1977-07-27. The listed applicant is J. Sklar Mfg. Co., Inc.. The 510(k) number is K771344.

When did GUSBERG HYSTERECTOMY CLAMP receive FDA 510(k) clearance?

GUSBERG HYSTERECTOMY CLAMP received FDA 510(k) clearance on 1977-07-27, under 510(k) number K771344.

Who is the listed applicant for GUSBERG HYSTERECTOMY CLAMP?

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

What is the FDA product code for GUSBERG HYSTERECTOMY CLAMP?

The FDA product code for GUSBERG HYSTERECTOMY CLAMP is HGC.

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Other records listing J. Sklar Mfg. Co., 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.

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Related Devices (Code: HGC)

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.

K891402UTERINE CLAMPSZinnanti Surgical Instruments, 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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