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FDA 510(k)

LAPAROSCOPY DRAPE, BOUNDARY

K-Number: K772301 · 1977-12-20

ApplicantProcter & Gamble Mfg. Co.
Decision Date1977-12-20
Product CodeFZT
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LAPAROSCOPY DRAPE, BOUNDARY is the device name listed in this FDA 510(k) record. The listed applicant is Procter & Gamble Mfg. Co.. It received FDA 510(k) clearance on 1977-12-20 under 510(k) number K772301. The device is classified under product code FZT. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LAPAROSCOPY DRAPE, BOUNDARY?

LAPAROSCOPY DRAPE, BOUNDARY is a medical device that received FDA 510(k) clearance on 1977-12-20. The listed applicant is Procter & Gamble Mfg. Co.. The 510(k) number is K772301.

When did LAPAROSCOPY DRAPE, BOUNDARY receive FDA 510(k) clearance?

LAPAROSCOPY DRAPE, BOUNDARY received FDA 510(k) clearance on 1977-12-20, under 510(k) number K772301.

Who is the listed applicant for LAPAROSCOPY DRAPE, BOUNDARY?

The FDA 510(k) record lists Procter & Gamble Mfg. Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LAPAROSCOPY DRAPE, BOUNDARY?

The FDA product code for LAPAROSCOPY DRAPE, BOUNDARY is FZT.

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Other records listing Procter & Gamble Mfg. Co. 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: FZT)

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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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